A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199612



Internal ID21338408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079876..95079969hg38UCSC Ensembl
chr8:96092104..96092197hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941465
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199612
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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