A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334424



Internal ID20867610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227802978..227879051hg38UCSC Ensembl
chr1:227990679..228066752hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3876074
hg1976074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059178
Samples
Known GenesPRSS38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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