A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957877



Internal ID16960064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125426565..125426712hg38UCSC Ensembl
Outerchr11:125296461..125296608hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002634
SamplesBILGI_BIOE
Known GenesPKNOX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957877
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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