A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv458826



Internal ID15172205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54791531..54868759hg38UCSC Ensembl
Innerchr19:55302983..55380214hg19UCSC Ensembl
Innerchr19:59994795..60072026hg18UCSC Ensembl
Innerchr19:59994795..60072026hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3877229
hg1977232
hg1877232
hg1777232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv438n27
Supporting Variantsnssv535711
SamplesNINDS_114
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv458826
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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