A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027708



Internal ID18770240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12477851..12518631hg38UCSC Ensembl
Innerchr7:12517477..12558257hg19UCSC Ensembl
Innerchr7:12484002..12524782hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3840781
hg1940781
hg1840781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6273n100
Supporting Variantsnssv3642974, nssv3642973, nssv3642972, nssv3642975
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)nsv1027708
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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