A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021080



Internal ID19110298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:63639341..63688050hg38UCSC Ensembl
Innerchr5:62935168..62983877hg19UCSC Ensembl
Innerchr5:62970924..63019633hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3848710
hg1948710
hg1848710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640786
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)nsv1021080
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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