A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755314



Internal ID18706909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72532208..72806109hg38UCSC Ensembl
Innerchr7:71997193..72276703hg19UCSC Ensembl
Innerchr7:71635129..71914639hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38273902
hg19279511
hg18279511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016734
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755314
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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