A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034945



Internal ID19124165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122203647..122293112hg38UCSC Ensembl
Innerchr7:121843701..121933166hg19UCSC Ensembl
Innerchr7:121630937..121720402hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3889466
hg1989466
hg1889466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6604n100
Supporting Variantsnssv3662124, nssv3751530
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)nsv1034945
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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