A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980563



Internal ID18856856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103014737..103014804hg38UCSC Ensembl
Outerchr9:105777019..105777086hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143379
Supporting Variants
SamplesKWS1
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980563
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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