A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695531



Internal ID15432183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44428364..44431738hg38UCSC Ensembl
Innerchr6:44396101..44399475hg19UCSC Ensembl
Innerchr6:44504079..44507453hg18UCSC Ensembl
Innerchr6:44504079..44507453hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383375
hg193375
hg183375
hg173375
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517370
Supporting Variants
Samples
Known GenesCDC5L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695531
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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