A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015769



Internal ID19104987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58013204..58042530hg38UCSC Ensembl
Innerchr5:57309031..57338357hg19UCSC Ensembl
Innerchr5:57344788..57374114hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3829327
hg1929327
hg1829327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642159, nssv3642158
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015769
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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