A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520601



Internal ID15447894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93027493..93031589hg38UCSC Ensembl
Innerchr15:93570723..93574819hg19UCSC Ensembl
Innerchr15:91371727..91375823hg18UCSC Ensembl
Innerchr15:91371727..91375823hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384097
hg194097
hg184097
hg174097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672983, nssv682287
Samples
Known GenesCHD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520601
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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