A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143556



Internal ID18932220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:6827635..6828936hg38UCSC Ensembl
Outerchr12:6936800..6938100hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381302
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980765
SamplesKWS1
Known GenesLEPREL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143556
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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