A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895994



Internal ID22671083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103708910..103734284hg38UCSC Ensembl
chr6:104156785..104182159hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3825375
hg1925375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895994
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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