A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063042



Internal ID18805573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42634891..42671142hg38UCSC Ensembl
Innerchr19:43139043..43175294hg19UCSC Ensembl
Innerchr19:47830883..47867134hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3836252
hg1936252
hg1836252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568652
Samples
Known GenesLIPE-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063042
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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