A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135749



Internal ID20702789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97698442..97877369hg38UCSC Ensembl
chr5:97034146..97213073hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38178928
hg19178928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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