A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021602



Internal ID19110820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150797535..150844521hg38UCSC Ensembl
Innerchr5:150177097..150224083hg19UCSC Ensembl
Innerchr5:150157290..150204276hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3846987
hg1946987
hg1846987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5818n100
Supporting Variantsnssv3746651
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)nsv1021602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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