A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119605



Internal ID18901405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:111483420..111484420hg38UCSC Ensembl
Outerchr9:114245700..114246700hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4125n106
Supporting Variantsnssv3982039
SamplesKWS1
Known GenesKIAA0368
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119605
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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