A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501877



Internal ID22559816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148641957..148645556hg38UCSC Ensembl
chr6:148963093..148966692hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501877
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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