A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957870



Internal ID17306743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36287192..36287305hg38UCSC Ensembl
Outerchr11:36308742..36308855hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005075
SamplesBILGI_BIOE
Known GenesCOMMD9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957870
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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