A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029018



Internal ID18771550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89106836..89527431hg38UCSC Ensembl
Innerchr7:88736150..89156745hg19UCSC Ensembl
Innerchr7:88574086..88994681hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38420596
hg19420596
hg18420596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655216
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029018
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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