A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119702



Internal ID19248654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:89776214..89776338hg38UCSC Ensembl
Outerchr1:90241773..90241897hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982157
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119702
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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