A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3756852



Internal ID19055133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42727697..42856259hg38UCSC Ensembl
Innerchr9:44114860..44243422hg19UCSC Ensembl
Innerchr9:44054856..44183418hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38128563
hg19128563
hg18128563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027972
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3756852
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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