A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696227



Internal ID15086193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48914136..48917927hg38UCSC Ensembl
Innerchr10:50122181..50125972hg19UCSC Ensembl
Innerchr10:49792187..49795978hg18UCSC Ensembl
Innerchr10:49792187..49795978hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383792
hg193792
hg183792
hg173792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517287
Supporting Variants
Samples
Known GenesLRRC18, WDFY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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