A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968411



Internal ID18896436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:33307299..33308099hg38UCSC Ensembl
Outerchr1:33772900..33773700hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136074
Supporting Variants
SamplesKWS2
Known GenesA3GALT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968411
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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