A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173552



Internal ID20740592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97693039..97697156hg38UCSC Ensembl
chr8:98705267..98709384hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384118
hg194118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425757
Supporting Variants
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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