A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026486



Internal ID1028302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62624859..62626508hg38UCSC Ensembl
Innerchr3:62624876..62626491hg38UCSC Ensembl
Outerchr3:62624842..62626525hg38UCSC Ensembl
chr3:62610534..62612183hg19UCSC Ensembl
Innerchr3:62610551..62612166hg19UCSC Ensembl
Outerchr3:62610517..62612200hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596375
Supporting Variants
SamplesNA19107
Known GenesCADPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026486
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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