A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750121



Internal ID15697391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69798188..69822699hg38UCSC Ensembl
Innerchr10:71557944..71582455hg19UCSC Ensembl
Innerchr10:71227950..71252461hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3824512
hg1924512
hg1824512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551478
Supporting Variants
Samples
Known GenesCOL13A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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