A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672983



Internal ID15409635
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520601
Supporting Variants
Samples
Known GenesCHD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672983
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer