A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113126



Internal ID18902925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:63301233..63301298hg38UCSC Ensembl
Outerchr1:63766904..63766969hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968022
SamplesKWS2
Known GenesLINC00466
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113126
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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