A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023128



Internal ID18765661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73420075..73571434hg38UCSC Ensembl
Innerchr7:72834405..72985764hg19UCSC Ensembl
Innerchr7:72472341..72623700hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38151360
hg19151360
hg18151360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n100
Supporting Variantsnssv3656489
Samples
Known GenesBAZ1B, BCL7B, FZD9, TBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023128
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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