A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114315



Internal ID18932242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:24750893..24750944hg38UCSC Ensembl
Outerchr22:25146860..25146911hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973821
SamplesKWS2
Known GenesPIWIL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114315
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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