A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112528



Internal ID18940583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:32266599..32266899hg38UCSC Ensembl
Outerchr1:32732200..32732500hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3966627
SamplesKWS2
Known GenesLCK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112528
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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