A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113156



Internal ID18911873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:111532072..111532183hg38UCSC Ensembl
Outerchr1:112074694..112074805hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985320, nssv3970596
SamplesKWS1, KWS2
Known GenesADORA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113156
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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