A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026894



Internal ID18769425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76524019..76674181hg38UCSC Ensembl
Innerchr7:76153336..76303498hg19UCSC Ensembl
Innerchr7:75991272..76141434hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38150163
hg19150163
hg18150163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6480n100
Supporting Variantsnssv3755349, nssv3656606, nssv3656605
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026894
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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