A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696677



Internal ID15086643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167323650..167357248hg38UCSC Ensembl
Innerchr6:167737138..167770736hg19UCSC Ensembl
Innerchr6:167657128..167690726hg18UCSC Ensembl
Innerchr6:167707549..167741147hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3833599
hg1933599
hg1833599
hg1733599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517210
Supporting Variants
Samples
Known GenesTTLL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696677
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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