A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150782



Internal ID18851473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:209761992..209762751hg38UCSC Ensembl
Outerchr1:209935337..209936096hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996258
SamplesKWB1
Known GenesTRAF3IP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150782
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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