A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695100



Internal ID15085066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1835882..1996938hg38UCSC Ensembl
Innerchr11:1857112..2018168hg19UCSC Ensembl
Innerchr11:1813688..1974744hg18UCSC Ensembl
Innerchr11:1813688..1974744hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38161057
hg19161057
hg18161057
hg17161057
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522320
Supporting Variants
Samples
Known GenesH19, LSP1, MIR4298, MIR675, MRPL23, MRPL23-AS1, SYT8, TNNI2, TNNT3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695100
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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