A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033914



Internal ID18776448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76479432..76671318hg38UCSC Ensembl
Innerchr7:76108749..76300635hg19UCSC Ensembl
Innerchr7:75946685..76138571hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38191887
hg19191887
hg18191887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6477n100
Supporting Variantsnssv3656521, nssv3656520, nssv3656519
Samples
Known GenesDTX2, LOC100133091, 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)nsv1033914
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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