A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136765



Internal ID18936257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:115820035..115820101hg38UCSC Ensembl
Outerchr3:115538882..115538948hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974662
SamplesKWS2
Known GenesLSAMP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136765
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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