A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507253



Internal ID22565201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62888708..62935825hg38UCSC Ensembl
chr6:63598613..63645730hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3847118
hg1947118
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507253
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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