A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060359



Internal ID18802890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:38022079..38061798hg38UCSC Ensembl
Innerchr19:38512719..38552438hg19UCSC Ensembl
Innerchr19:43204559..43244278hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3839720
hg1939720
hg1839720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724532
Samples
Known GenesSIPA1L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060359
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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