A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057681



Internal ID21966914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74732103..74732103hg38UCSC Ensembl
chr1:75197787..75197787hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524399
Samples
Known GenesCRYZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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