A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967959



Internal ID18892558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:6371544..6371611hg38UCSC Ensembl
Outerchr1:6431604..6431671hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113068
Supporting Variants
SamplesKWS2
Known GenesACOT7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967959
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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