A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702742



Internal ID15439394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25286135..25287439hg38UCSC Ensembl
Innerchr13:25860273..25861577hg19UCSC Ensembl
Innerchr13:24758273..24759577hg18UCSC Ensembl
Innerchr13:24758273..24759577hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381305
hg191305
hg181305
hg171305
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526439
Supporting Variants
Samples
Known GenesMTMR6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702742
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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