A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063975



Internal ID20631015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74714265..74726826hg38UCSC Ensembl
chr1:75179949..75192510hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3812562
hg1912562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324398
Supporting Variants
Samples
Known GenesCRYZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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