A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135959



Internal ID19275350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:11034447..11034539hg38UCSC Ensembl
Outerchr6:11034680..11034772hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989557
SamplesKWS2
Known GenesELOVL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135959
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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