A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436250



Internal ID22494120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38699842..38699891hg38UCSC Ensembl
chr6:38667618..38667667hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894589
Supporting Variants
Samples
Known GenesGLO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436250
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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