A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057509



Internal ID19146728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53773463..53814770hg38UCSC Ensembl
Innerchr20:52390002..52431309hg19UCSC Ensembl
Innerchr20:51823409..51864716hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3841308
hg1941308
hg1841308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731368
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)nsv1057509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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