A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676701



Internal ID15413353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44428364..44454952hg38UCSC Ensembl
Innerchr6:44396101..44422689hg19UCSC Ensembl
Innerchr6:44504079..44530667hg18UCSC Ensembl
Innerchr6:44504079..44530667hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3826589
hg1926589
hg1826589
hg1726589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517370
Supporting Variants
Samples
Known GenesCDC5L, MIR4642
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676701
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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