A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643583



Internal ID7030342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7386153..7389218hg38UCSC Ensembl
Innerchr19:7386158..7389214hg38UCSC Ensembl
Outerchr19:7386149..7389223hg38UCSC Ensembl
chr19:7451039..7454104hg19UCSC Ensembl
Innerchr19:7451044..7454100hg19UCSC Ensembl
Outerchr19:7451035..7454109hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383066
hg193066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15987272, essv15987273, essv15987267, essv15987250, essv15987266, essv15987249, essv15987258, essv15987251, essv15987269, essv15987271, essv15987248, essv15987262, essv15987252, essv15987247, essv15987256, essv15987254, essv15987257, essv15987268, essv15987264, essv15987260, essv15987265, essv15987253, essv15987255, essv15987246, essv15987259, essv15987270, essv15987261, essv15987263
SamplesHG03857, NA21097, NA20529, HG00231, HG03960, HG01359, HG03237, HG04202, HG01326, NA12045, HG03944, NA20894, HG03782, NA19771, HG03911, NA20910, HG03887, HG03595, NA20535, HG04235, HG01613, NA20821, HG03702, HG02230, HG00267, HG04153, HG03931, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643583
Frequency
Sample Size2504
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer