A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100007



Internal ID20667047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44340603..44345351hg38UCSC Ensembl
chr3:44382095..44386843hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384749
hg194749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372831
Supporting Variants
Samples
Known GenesTCAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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