A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020877



Internal ID19110095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84867945..84906954hg38UCSC Ensembl
Innerchr5:84163763..84202772hg19UCSC Ensembl
Innerchr5:84199519..84238528hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3839010
hg1939010
hg1839010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5712n100
Supporting Variantsnssv3747337
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)nsv1020877
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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