A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123509



Internal ID19260807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21155853..21157948hg38UCSC Ensembl
Outerchr13:21729992..21732087hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv924n106
Supporting Variantsnssv3973274
SamplesKWS1
Known GenesSKA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123509
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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