A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071485



Internal ID21980718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:151969579..151969579hg38UCSC Ensembl
chr7:151666664..151666664hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566214
Samples
Known GenesGALNTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071485
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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