A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24187



Internal ID15840374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36269972..36308343hg38UCSC Ensembl
Outerchr19:36238786..36315117hg38UCSC Ensembl
Innerchr19:36760874..36799245hg19UCSC Ensembl
Outerchr19:36729688..36806019hg19UCSC Ensembl
Innerchr19:41452714..41491085hg18UCSC Ensembl
Outerchr19:41421528..41497859hg18UCSC Ensembl
Innerchr19:41452714..41491085hg17UCSC Ensembl
Outerchr19:41421528..41497859hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3876332
hg1976332
hg1876332
hg1776332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9715
Supporting Variants
SamplesNA18975
Known GenesLINC00665, LOC100134317
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv24187
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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