A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137467



Internal ID19248530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69868282..69868350hg38UCSC Ensembl
Outerchr9:72483198..72483266hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986939, nssv3976160
SamplesKWS2, KWS1
Known GenesC9orf135
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137467
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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