A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982360



Internal ID19223013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136033354..136055154hg38UCSC Ensembl
Outerchr9:138925200..138947000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821801
hg1921801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145273
Supporting Variants
SamplesKWS1
Known GenesNACC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982360
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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