A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025397



Internal ID19114615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12503535..12572434hg38UCSC Ensembl
Innerchr7:12543161..12612059hg19UCSC Ensembl
Innerchr7:12509686..12578584hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3868900
hg1968899
hg1868899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6276n100
Supporting Variantsnssv3642980
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)nsv1025397
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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