A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994980



Internal ID19208229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:178400..180600hg38UCSC Ensembl
Outerchr9:178400..180600hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144247
Supporting Variants
SamplesKWS1
Known GenesCBWD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994980
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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