A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655716



Internal ID18607311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72532208..72859219hg38UCSC Ensembl
Innerchr7:71997193..72329779hg19UCSC Ensembl
Innerchr7:71635129..71967715hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38327012
hg19332587
hg18332587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026868
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655716
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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