A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024364



Internal ID19113581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122203647..122276737hg38UCSC Ensembl
Innerchr7:121843701..121916791hg19UCSC Ensembl
Innerchr7:121630937..121704027hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3873091
hg1973091
hg1873091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6604n100
Supporting Variantsnssv3751529
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)nsv1024364
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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