A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063261



Internal ID19152480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43029369..43232095hg38UCSC Ensembl
Innerchr19:43533521..43736247hg19UCSC Ensembl
Innerchr19:48225361..48428087hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38202727
hg19202727
hg18202727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3583n100
Supporting Variantsnssv3571749
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063261
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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