A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500952



Internal ID22558889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114429989..114510231hg38UCSC Ensembl
chr6:114751153..114831395hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3880243
hg1980243
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843663
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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