A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062518



Internal ID18805049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:38049814..38074273hg38UCSC Ensembl
Innerchr19:38540454..38564913hg19UCSC Ensembl
Innerchr19:43232294..43256753hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3824460
hg1924460
hg1824460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568196
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)nsv1062518
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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