A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026017



Internal ID19115234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8704114..8746922hg38UCSC Ensembl
Innerchr5:8704226..8747034hg19UCSC Ensembl
Innerchr5:8757226..8800034hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3842809
hg1942809
hg1842809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3638095
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)nsv1026017
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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