A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002043



Internal ID18845733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69163008..69163332hg38UCSC Ensembl
Outerchr9:71777924..71778248hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151110
Supporting Variants
SamplesKWB1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002043
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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