A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657087



Internal ID18955368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76819246..77118682hg38UCSC Ensembl
Innerchr7:76448563..76747999hg19UCSC Ensembl
Innerchr7:76286499..76585935hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38299437
hg19299437
hg18299437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018360
Supporting Variants
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657087
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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