A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027594



Internal ID19116813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..63246026hg38UCSC Ensembl
Innerchr7:61875418..62706404hg19UCSC Ensembl
Innerchr7:61512853..62343839hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38739247
hg19830987
hg18830987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661763
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)nsv1027594
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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