A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506558



Internal ID22564506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56042879..56047978hg38UCSC Ensembl
chr6:55907677..55912776hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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