A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764062



Internal ID3765878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42584089..42655641hg38UCSC Ensembl
chr10:43079537..43151089hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3871553
hg1971553
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623018
Supporting Variants
SamplesNA20804
Known GenesZNF33B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764062
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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