A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056616



Internal ID19145835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22061780..22174297hg38UCSC Ensembl
Innerchr20:22042418..22154935hg19UCSC Ensembl
Innerchr20:21990418..22102935hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38112518
hg19112518
hg18112518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4285n100
Supporting Variantsnssv3584655
Samples
Known GenesLOC100270679
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056616
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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