A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587175



Internal ID6974602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110929985..110935133hg38UCSC Ensembl
Innerchr1:110929985..110935133hg38UCSC Ensembl
Outerchr1:110929715..110935410hg38UCSC Ensembl
chr1:111472607..111477755hg19UCSC Ensembl
Innerchr1:111472607..111477755hg19UCSC Ensembl
Outerchr1:111472337..111478032hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385149
hg195149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10064533, essv10064527, essv10064536, essv10064526, essv10064531, essv10064535, essv10064529, essv10064534, essv10064530, essv10064528, essv10064532
SamplesHG02026, HG00566, HG01873, HG02155, NA18635, HG00590, HG02512, HG02187, HG00419, HG00692, HG01596
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587175
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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