A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133567



Internal ID19258431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194486571..194487171hg38UCSC Ensembl
Outerchr3:194207300..194207900hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969131
SamplesKWS2
Known GenesLINC00884
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133567
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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