A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676648



Internal ID15413300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44428364..44454729hg38UCSC Ensembl
Innerchr6:44396101..44422466hg19UCSC Ensembl
Innerchr6:44504079..44530444hg18UCSC Ensembl
Innerchr6:44504079..44530444hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3826366
hg1926366
hg1826366
hg1726366
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv676648
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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