A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123692



Internal ID18927167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136031939..136032002hg38UCSC Ensembl
Outerchr3:135750781..135750844hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973465
SamplesKWS2
Known GenesPPP2R3A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123692
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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