A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701682



Internal ID15438334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113052193..113100572hg38UCSC Ensembl
Innerchr9:115814473..115862852hg19UCSC Ensembl
Innerchr9:114854294..114902673hg18UCSC Ensembl
Innerchr9:112894028..112942406hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3848380
hg1948380
hg1848380
hg1748379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525545
Supporting Variants
Samples
Known GenesZFP37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701682
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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