A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724626



Internal ID18676221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43159205..43342230hg38UCSC Ensembl
Innerchr19:43663357..43846382hg19UCSC Ensembl
Innerchr19:48355197..48538222hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38183026
hg19183026
hg18183026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062704
Supporting Variants
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724626
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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