A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13964374



Internal ID3534715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126025003..126025643hg38UCSC Ensembl
Innerchr10:126025022..126025624hg38UCSC Ensembl
Outerchr10:126024984..126025662hg38UCSC Ensembl
chr10:127713572..127714212hg19UCSC Ensembl
Innerchr10:127713591..127714193hg19UCSC Ensembl
Outerchr10:127713553..127714231hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624848
Supporting Variants
SamplesHG03124
Known GenesADAM12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13964374
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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