A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660342



Internal ID15396994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156383446..156392367hg38UCSC Ensembl
Innerchr4:157304598..157313519hg19UCSC Ensembl
Innerchr4:157524048..157532969hg18UCSC Ensembl
Innerchr4:157662203..157671124hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg388922
hg198922
hg188922
hg178922
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517773
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660342
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