A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032928



Internal ID19122150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146525085..146563200hg38UCSC Ensembl
Innerchr7:146222177..146260292hg19UCSC Ensembl
Innerchr7:145853110..145891225hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3838116
hg1938116
hg1838116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6747n100
Supporting Variantsnssv3757715
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032928
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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