A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092317



Internal ID20659358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104069601..104071400hg38UCSC Ensembl
chr3:103788445..103790244hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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