A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118077



Internal ID18918502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:37292292..37322228hg38UCSC Ensembl
Outerchr22:37688333..37718269hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3829937
hg1929937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980286
SamplesKWS1
Known GenesCYTH4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118077
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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