A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616984



Internal ID18915265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195799700..195982791hg38UCSC Ensembl
Innerchr3:195526571..195709662hg19UCSC Ensembl
Innerchr3:197010968..197194059hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38183092
hg19183092
hg18183092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005193
Supporting Variants
Samples
Known GenesMIR6829, MUC4, SDHAP1, TNK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616984
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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