A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956936



Internal ID22732089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74727205..74727205hg38UCSC Ensembl
chr1:75192889..75192889hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369998
Samples
Known GenesCRYZ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956936
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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