A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660040



Internal ID15396692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44428364..44453503hg38UCSC Ensembl
Innerchr6:44396101..44421240hg19UCSC Ensembl
Innerchr6:44504079..44529218hg18UCSC Ensembl
Innerchr6:44504079..44529218hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3825140
hg1925140
hg1825140
hg1725140
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)nssv660040
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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