A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913284



Internal ID5334945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101596213..101596871hg38UCSC Ensembl
Innerchr10:101596213..101596871hg38UCSC Ensembl
Outerchr10:101595839..101597117hg38UCSC Ensembl
chr10:103355970..103356628hg19UCSC Ensembl
Innerchr10:103355970..103356628hg19UCSC Ensembl
Outerchr10:103355596..103356874hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624385
Supporting Variants
SamplesNA18874
Known GenesDPCD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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