A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130909



Internal ID19286516
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 StatusM
Merged Variants
Supporting Variantsnssv3980586, nssv3966590
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130909
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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