A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584844



Internal ID18536439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45713700..45754523hg38UCSC Ensembl
Innerchr20:44342339..44383162hg19UCSC Ensembl
Innerchr20:43775753..43816569hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3840824
hg1940824
hg1840817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065614
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)nssv3584844
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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