A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507313



Internal ID22565261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65923201..65965064hg38UCSC Ensembl
chr6:66633094..66674957hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3841864
hg1941864
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507313
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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