A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033715



Internal ID18776248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76445651..76803016hg38UCSC Ensembl
Innerchr7:76074968..76432333hg19UCSC Ensembl
Innerchr7:75912904..76270269hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38357366
hg19357366
hg18357366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6472n100
Supporting Variantsnssv3656515
Samples
Known GenesDTX2, FDPSP2, 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)nsv1033715
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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