A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155932



Internal ID15508415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156944011..157023277hg38UCSC Ensembl
Innerchr7:156736705..156815971hg19UCSC Ensembl
Innerchr7:156429466..156508732hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3879267
hg1979267
hg1879267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609210
Supporting Variants
Samples1780862444_A
Known GenesMNX1, MNX1-AS1, NOM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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