A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029240



Internal ID19118459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62559778..63246026hg38UCSC Ensembl
Innerchr7:62020156..62706404hg19UCSC Ensembl
Innerchr7:61657591..62343839hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38686249
hg19686249
hg18686249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661840, nssv3661839
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)nsv1029240
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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