A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030043



Internal ID19119262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19323743..19402605hg38UCSC Ensembl
Innerchr5:19323852..19402714hg19UCSC Ensembl
Innerchr5:19359609..19438471hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3878863
hg1978863
hg1878863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635909
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)nsv1030043
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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