A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987619



Internal ID19209479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:96153063..96153123hg38UCSC Ensembl
Outerchr1:96618619..96618679hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132826
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987619
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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