A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018805



Internal ID19108022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135705961..135730733hg38UCSC Ensembl
Innerchr5:135041650..135066422hg19UCSC Ensembl
Innerchr5:135069549..135094321hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3824773
hg1924773
hg1824773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5811n100
Supporting Variantsnssv3648124, nssv3648125
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)nsv1018805
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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