A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325617



Internal ID20858748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221570601..221582600hg38UCSC Ensembl
chr1:221743943..221755942hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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