A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888002



Internal ID22663002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112594043..112609630hg38UCSC Ensembl
chr6:112915245..112930832hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3815588
hg1915588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888002
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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