A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968021



Internal ID18879424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:63239685..63242475hg38UCSC Ensembl
Outerchr1:63705356..63708146hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382791
hg192791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113125
Supporting Variants
SamplesKWS2
Known GenesLINC00466
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968021
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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