A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501672



Internal ID22559611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157245360..157262351hg38UCSC Ensembl
chr6:157617282..157634273hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3816992
hg1916992
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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