A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018967



Internal ID19108184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64857751..64920491hg38UCSC Ensembl
Innerchr7:64318129..64380869hg19UCSC Ensembl
Innerchr7:63955564..64018304hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3862741
hg1962741
hg1862741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655506
Samples
Known GenesZNF273
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018967
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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