A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951036



Internal ID17299910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:71786855..71802154hg38UCSC Ensembl
Outerchr11:71497901..71513200hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3815300
hg1915300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999583
SamplesBILGI_BIOE
Known GenesALG1L9P, FAM86C1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951036
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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