A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661444



Internal ID18959725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..56886690hg38UCSC Ensembl
Innerchr7:56807732..56954387hg19UCSC Ensembl
Innerchr7:56775226..56921881hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38146652
hg19146656
hg18146656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027491
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)nssv3661444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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