A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643462



Internal ID6683536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3393625..3395166hg38UCSC Ensembl
Innerchr19:3393664..3395127hg38UCSC Ensembl
Outerchr19:3393586..3395205hg38UCSC Ensembl
chr19:3393623..3395164hg19UCSC Ensembl
Innerchr19:3393662..3395125hg19UCSC Ensembl
Outerchr19:3393584..3395203hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15974571, essv15974572, essv15974576, essv15974573, essv15974575, essv15974570, essv15974569, essv15974574
SamplesHG03703, HG03611, HG03604, HG03895, NA21112, HG03238, NA20899, HG03950
Known GenesNFIC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643462
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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