A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662196



Internal ID18960477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131347777..131422147hg38UCSC Ensembl
Innerchr7:131032536..131106906hg19UCSC Ensembl
Innerchr7:130683076..130757446hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3874371
hg1974371
hg1874371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032787
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)nssv3662196
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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