A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503779



Internal ID22561720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21499680..21504509hg38UCSC Ensembl
chr6:21499911..21504740hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384830
hg194830
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845183
Supporting Variants
Samples
Known GenesLINC00581
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503779
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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