A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150969



Internal ID15875522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63522433..63566995hg38UCSC Ensembl
Innerchr20:62153786..62198348hg19UCSC Ensembl
Innerchr20:61624230..61668792hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844563
hg1944563
hg1844563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586570
Supporting Variants
SamplesHGDP00696
Known GenesC20orf195, HELZ2, PTK6, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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