A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755931



Internal ID18707526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33296370..33574894hg38UCSC Ensembl
Innerchr9:33296368..33574892hg19UCSC Ensembl
Innerchr9:33286368..33564892hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38278525
hg19278525
hg18278525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024207
Supporting Variants
Samples
Known GenesANKRD18B, AQP3, AQP7, MIR6851, NFX1, NOL6, SUGT1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755931
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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