A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019588



Internal ID19108806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:100298059..100513939hg38UCSC Ensembl
Innerchr5:99633763..99849643hg19UCSC Ensembl
Innerchr5:99661662..99877542hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38215881
hg19215881
hg18215881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5737n100
Supporting Variantsnssv3645772
Samples
Known GenesLOC100133050
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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