A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142591



Internal ID18929751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:185911072..185991507hg38UCSC Ensembl
Outerchr3:185628860..185709296hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3880436
hg1980437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994078
SamplesKWS1
Known GenesLOC344887, TRA2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142591
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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