A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136671



Internal ID18935257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:33355629..33355780hg38UCSC Ensembl
Outerchr22:33751615..33751766hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956550, nssv3973360
SamplesKWS1, KWS2
Known GenesLARGE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136671
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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