A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704560



Internal ID15441212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185117420..185117503hg38UCSC Ensembl
Innerchr4:186038574..186038657hg19UCSC Ensembl
Innerchr4:186275568..186275651hg18UCSC Ensembl
Innerchr4:186413723..186413806hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
hg1884
hg1784
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704560
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