A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325159



Internal ID20858289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93186701..93188000hg38UCSC Ensembl
chr1:93652258..93653557hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065557
Samples
Known GenesCCDC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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