A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626365



Internal ID15503212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26134091..26138014hg38UCSC Ensembl
Outerchr1:26123610..26141503hg38UCSC Ensembl
Innerchr1:26460582..26464505hg19UCSC Ensembl
Outerchr1:26450101..26467994hg19UCSC Ensembl
Innerchr1:26333169..26337092hg18UCSC Ensembl
Outerchr1:26322688..26340581hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817894
hg1917894
hg1817894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511129
Supporting Variants
Samples1
Known GenesPDIK1L
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626365
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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