A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752988



Internal ID19051269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62997085hg38UCSC Ensembl
Innerchr7:61063962..62457463hg19UCSC Ensembl
Innerchr7:61067904..62094898hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381915849
hg191393502
hg181026995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017907
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)nssv3752988
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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