A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642985



Internal ID18941266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12643514..12659431hg38UCSC Ensembl
Innerchr7:12683139..12699056hg19UCSC Ensembl
Innerchr7:12649664..12665581hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3815918
hg1915918
hg1815918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019962
Supporting Variants
Samples
Known GenesSCIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642985
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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