A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584683



Internal ID18882964
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 StatusS
Merged Variantsnsv1059041
Supporting Variants
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)nssv3584683
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer