A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662189



Internal ID18960470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131332669..131375946hg38UCSC Ensembl
Innerchr7:131017428..131060705hg19UCSC Ensembl
Innerchr7:130667968..130711245hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3843278
hg1943278
hg1843278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021328
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)nssv3662189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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