A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119612



Internal ID19274126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133551778..133588478hg38UCSC Ensembl
Outerchr9:136416900..136453600hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3836701
hg1936701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4157n106
Supporting Variantsnssv3982046
SamplesKWS1
Known GenesADAMTSL2, FAM163B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119612
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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