A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152339



Internal ID18852717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:95196624..95196712hg38UCSC Ensembl
Outerchr13:95848878..95848966hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996941
SamplesKWB1
Known GenesABCC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152339
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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