A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966590



Internal ID19241072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:33123437..33136632hg38UCSC Ensembl
Outerchr12:33276371..33289566hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3813196
hg1913196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130909
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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