A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122974



Internal ID19251309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64086236..64086303hg38UCSC Ensembl
Outerchr15:64378435..64378502hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971570
SamplesKWS2
Known GenesFAM96A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122974
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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