A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059041



Internal ID19148260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25851469..26026633hg38UCSC Ensembl
Innerchr20:25832105..26007269hg19UCSC Ensembl
Innerchr20:25780105..25955269hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38175165
hg19175165
hg18175165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584683
Samples
Known GenesLOC100134868
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059041
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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