A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124465



Internal ID18918533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113248246..113248309hg38UCSC Ensembl
Outerchr9:116010526..116010589hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976944, nssv3960406
SamplesKWS1, KWS2
Known GenesSLC31A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124465
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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