A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524197



Internal ID15104804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79919554..79923673hg38UCSC Ensembl
Innerchr15:80211896..80216015hg19UCSC Ensembl
Innerchr15:77998951..78003070hg18UCSC Ensembl
Innerchr15:77998951..78003070hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384120
hg194120
hg184120
hg174120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155n21
Supporting Variantsnssv700081
Samples
Known GenesC15orf37, ST20, ST20-MTHFS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524197
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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