A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062040



Internal ID18804571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37803825..37879816hg38UCSC Ensembl
Innerchr19:38294465..38370456hg19UCSC Ensembl
Innerchr19:42986305..43062296hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3875992
hg1975992
hg1875992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568194
Samples
Known GenesLOC100631378, LOC644554
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062040
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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