A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502531



Internal ID22560472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161593523..161624249hg38UCSC Ensembl
chr6:162014555..162045281hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3830727
hg1930727
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844158
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502531
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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