A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968388



Internal ID18879388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1348520..1351320hg38UCSC Ensembl
Outerchr1:1283900..1286700hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121739
Supporting Variants
SamplesKWS2
Known GenesDVL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968388
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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