A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507233



Internal ID22565181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61534235..61558193hg38UCSC Ensembl
chr6:62244140..62268098hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3823959
hg1923959
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507233
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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