A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113089



Internal ID18938171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24211928..24212027hg38UCSC Ensembl
Outerchr1:24538418..24538517hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970517, nssv3995115
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113089
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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