A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015654



Internal ID19104872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114592587..114640320hg38UCSC Ensembl
Innerchr5:113928284..113976017hg19UCSC Ensembl
Innerchr5:113956183..114003916hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3847734
hg1947734
hg1847734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5785n100
Supporting Variantsnssv3746585
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)nsv1015654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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