A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13750236



Internal ID4766196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32659704..32676403hg38UCSC Ensembl
Innerchr10:32659704..32676403hg38UCSC Ensembl
Outerchr10:32659204..32676903hg38UCSC Ensembl
chr10:32948632..32965331hg19UCSC Ensembl
Innerchr10:32948632..32965331hg19UCSC Ensembl
Outerchr10:32948132..32965831hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3816700
hg1916700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622834
Supporting Variants
SamplesNA11832
Known GenesCCDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13750236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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