A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662202



Internal ID18960483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131371882..131447596hg38UCSC Ensembl
Innerchr7:131056641..131132355hg19UCSC Ensembl
Innerchr7:130707181..130782895hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3875715
hg1975715
hg1875715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019529
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)nssv3662202
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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