A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331845



Internal ID20865012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170753730..170754327hg38UCSC Ensembl
chr1:170722871..170723468hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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