A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666796



Internal ID15056762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87265357..87307076hg38UCSC Ensembl
Innerchr4:88186509..88228228hg19UCSC Ensembl
Innerchr4:88405533..88447252hg18UCSC Ensembl
Innerchr4:88543688..88585407hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3841720
hg1941720
hg1841720
hg1741720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516203
Supporting Variants
Samples
Known GenesHSD17B13, MIR5705
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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