A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643242



Internal ID18941523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19158481..19185179hg38UCSC Ensembl
Innerchr7:19198104..19224802hg19UCSC Ensembl
Innerchr7:19164629..19191327hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3826699
hg1926699
hg1826699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019418
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643242
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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