A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13757265



Internal ID3009866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38042306..38044799hg38UCSC Ensembl
Innerchr10:38042349..38044757hg38UCSC Ensembl
Outerchr10:38042264..38044842hg38UCSC Ensembl
chr10:38331234..38333727hg19UCSC Ensembl
Innerchr10:38331277..38333685hg19UCSC Ensembl
Outerchr10:38331192..38333770hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg382494
hg192494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622975
Supporting Variants
SamplesHG02652
Known GenesZNF33A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13757265
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