A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907492



Internal ID22682701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82476193..82476269hg38UCSC Ensembl
chr6:83185910..83185986hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907492
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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