A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705818



Internal ID15095784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117907364..117919522hg38UCSC Ensembl
Innerchr6:118228527..118240685hg19UCSC Ensembl
Innerchr6:118335220..118347378hg18UCSC Ensembl
Innerchr6:118335220..118347378hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3812159
hg1912159
hg1812159
hg1712159
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522455
Supporting Variants
Samples
Known GenesSLC35F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705818
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer