A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140214



Internal ID15646714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98909352..98953316hg38UCSC Ensembl
Innerchr9:101671634..101715598hg19UCSC Ensembl
Innerchr9:100711455..100755419hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3843965
hg1943965
hg1843965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614953
Supporting Variants
Samples
Known GenesCOL15A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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