A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697396



Internal ID15434048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44374003..44375477hg38UCSC Ensembl
Innerchr4:44376020..44377494hg19UCSC Ensembl
Innerchr4:44070777..44072251hg18UCSC Ensembl
Innerchr4:44216948..44218422hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg381475
hg191475
hg181475
hg171475
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520405
Supporting Variants
Samples
Known GenesKCTD8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697396
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