A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004085



Internal ID21913428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39909266..39909330hg38UCSC Ensembl
chr6:39877010..39877074hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568016
Samples
Known GenesMOCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004085
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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