A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018839



Internal ID19108056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702410..8746922hg38UCSC Ensembl
Innerchr5:8702522..8747034hg19UCSC Ensembl
Innerchr5:8755522..8800034hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844513
hg1944513
hg1844513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3639694, nssv3639693, nssv3639695, nssv3639692, nssv3746304
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)nsv1018839
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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