A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584843



Internal ID18536438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45713700..45749572hg38UCSC Ensembl
Innerchr20:44342339..44378211hg19UCSC Ensembl
Innerchr20:43775753..43811618hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3835873
hg1935873
hg1835866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066695
Supporting Variants
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584843
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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