A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701744



Internal ID15091710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167323650..167354325hg38UCSC Ensembl
Innerchr6:167737138..167767813hg19UCSC Ensembl
Innerchr6:167657128..167687803hg18UCSC Ensembl
Innerchr6:167707549..167738224hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3830676
hg1930676
hg1830676
hg1730676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv701744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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