A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662197



Internal ID18960478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131360548..131419987hg38UCSC Ensembl
Innerchr7:131045307..131104746hg19UCSC Ensembl
Innerchr7:130695847..130755286hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3859440
hg1959440
hg1859440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033636
Supporting Variants
Samples
Known GenesMKLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662197
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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