A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329986



Internal ID20863140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187440157..187500184hg38UCSC Ensembl
chr1:187409289..187469316hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3860028
hg1960028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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