A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118949



Internal ID19257363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:32654814..32694514hg38UCSC Ensembl
Outerchr22:33050800..33090500hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3839701
hg1939701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2454n106
Supporting Variantsnssv3981736
SamplesKWS1
Known GenesSYN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118949
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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