A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094106



Internal ID20661146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127611674..127612000hg38UCSC Ensembl
chr3:127330517..127330843hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356113
Supporting Variants
Samples
Known GenesMCM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02049


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