A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656493



Internal ID18954774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76051175..76190114hg38UCSC Ensembl
Innerchr7:75680493..75819432hg19UCSC Ensembl
Innerchr7:75518429..75657368hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38138940
hg19138940
hg18138940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033450
Supporting Variants
Samples
Known GenesMDH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656493
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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