A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511126



Internal ID15503865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15825802..15827390hg38UCSC Ensembl
Outerchr1:15822806..15835341hg38UCSC Ensembl
Innerchr1:16152297..16153885hg19UCSC Ensembl
Outerchr1:16149301..16161836hg19UCSC Ensembl
Innerchr1:16024884..16026472hg18UCSC Ensembl
Outerchr1:16021888..16034423hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3812536
hg1912536
hg1812536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626032
Samples1
Known GenesFLJ37453
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511126
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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