A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150970



Internal ID15880926
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
SamplesNINDS_49
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)nssv1150970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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