A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077001



Internal ID21986234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160599559..160599559hg38UCSC Ensembl
chr5:160026566..160026566hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568796
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077001
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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