A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020236



Internal ID18762772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6209299..6650746hg38UCSC Ensembl
Innerchr7:6248930..6690377hg19UCSC Ensembl
Innerchr7:6215455..6656902hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38441448
hg19441448
hg18441448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655073
Samples
Known GenesC7orf26, CYTH3, DAGLB, FAM220A, GRID2IP, KDELR2, RAC1, ZDHHC4, ZNF316, ZNF853
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020236
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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