A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661462



Internal ID18959743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..56940122hg38UCSC Ensembl
Innerchr7:56807732..57007829hg19UCSC Ensembl
Innerchr7:56775226..57011771hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38200084
hg19200098
hg18236546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026656
Supporting Variants
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661462
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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