A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999591



Internal ID16945857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:76158957..76208556hg38UCSC Ensembl
Outerchr11:75870001..75919600hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3849600
hg1949600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951044
Supporting Variants
SamplesBILGI_BIOE
Known GenesWNT11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999591
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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