A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003998



Internal ID21913341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71184191..71224534hg38UCSC Ensembl
chr6:71893894..71934237hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3840344
hg1940344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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