A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449563



Internal ID22507433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2863313..2867635hg38UCSC Ensembl
chr6:2863547..2867869hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384323
hg194323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906542
Supporting Variants
Samples
Known GenesMGC39372
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449563
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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