A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1652777



Internal ID15490070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51639362..51644944hg38UCSC Ensembl
Innerchr19:52142615..52148197hg19UCSC Ensembl
Innerchr19:56834427..56840009hg18UCSC Ensembl
Innerchr19:56834427..56840009hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385583
hg195583
hg185583
hg175583
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv442771
Supporting Variants
SamplesNA19007
Known GenesSIGLEC14
MethodSNP array
AnalysisWe used two computational approaches to identify CNVs: the hidden Markov model Birdseye, and an approach based on correlation between nearby probes across a population sample. To maximize the quality of reported findings, we ran duplicate experiments in independent labs, and report the CNVs that were observed in both experiments, in the same samples and at essentially identical genomic locations.
Platform[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
Comments
ReferenceMcCarroll_et_al_2008
Pubmed ID18776908
Accession Number(s)nssv1652777
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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