A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023588



Internal ID19112805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155036026..155084895hg38UCSC Ensembl
Innerchr5:154415586..154464455hg19UCSC Ensembl
Innerchr5:154395779..154444648hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3848870
hg1948870
hg1848870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648194
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)nsv1023588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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