A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689134



Internal ID15425786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44428364..44451599hg38UCSC Ensembl
Innerchr6:44396101..44419336hg19UCSC Ensembl
Innerchr6:44504079..44527314hg18UCSC Ensembl
Innerchr6:44504079..44527314hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3823236
hg1923236
hg1823236
hg1723236
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)nssv689134
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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