A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065537



Internal ID19154756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47805204..47821109hg38UCSC Ensembl
Innerchr20:46433948..46449853hg19UCSC Ensembl
Innerchr20:45867355..45883260hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3815906
hg1915906
hg1815906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584947, nssv3584948
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065537
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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