A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897313



Internal ID22672414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53938061..53938126hg38UCSC Ensembl
chr6:53802859..53802924hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897313
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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