A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124729



Internal ID19254088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:99025992..99026095hg38UCSC Ensembl
Outerchr13:99678246..99678349hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1022n106
Supporting Variantsnssv3976783
SamplesKWS1
Known GenesDOCK9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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