A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135136



Internal ID19274033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:49160305..49160643hg38UCSC Ensembl
Outerchr3:49197738..49198076hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2523n106
Supporting Variantsnssv3988688
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135136
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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