A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696142



Internal ID18994423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64866653hg38UCSC Ensembl
Innerchr9:69505934..69879071hg19UCSC Ensembl
Innerchr9:68795754..69168891hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38373138
hg19373138
hg18373138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034953
Supporting Variants
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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