A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990178



Internal ID19232620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135479254..135480254hg38UCSC Ensembl
Outerchr9:138371100..138372100hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122248
Supporting Variants
SamplesKWS2
Known GenesPPP1R26
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990178
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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