A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032746



Internal ID19121968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58379644..58405721hg38UCSC Ensembl
Innerchr5:57675471..57701548hg19UCSC Ensembl
Innerchr5:57711228..57737305hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3826078
hg1926078
hg1826078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747206
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)nsv1032746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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