A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677144



Internal ID15067110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15018884hg38UCSC Ensembl
Innerchr10:14990369..15060883hg19UCSC Ensembl
Innerchr10:15030375..15100889hg18UCSC Ensembl
Innerchr10:15030375..15100889hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870515
hg1970515
hg1870515
hg1770515
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520429
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677144
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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