A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968024



Internal ID18891170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:63475910..63475981hg38UCSC Ensembl
Outerchr1:63941581..63941652hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113128
Supporting Variants
SamplesKWS2
Known GenesITGB3BP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968024
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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