A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705112



Internal ID15441764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59284839..59290579hg38UCSC Ensembl
Innerchr10:61044599..61050339hg19UCSC Ensembl
Innerchr10:60714605..60720345hg18UCSC Ensembl
Innerchr10:60714605..60720345hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385741
hg195741
hg185741
hg175741
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528505
Supporting Variants
Samples
Known GenesFAM13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705112
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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