A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017294



Internal ID19106511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90556754..90593974hg38UCSC Ensembl
Innerchr7:90186068..90223288hg19UCSC Ensembl
Innerchr7:90024004..90061224hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3837221
hg1937221
hg1837221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6533n100
Supporting Variantsnssv3655236
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)nsv1017294
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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