A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756308



Internal ID20532168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160635265..160635265hg38UCSC Ensembl
chr5:160062272..160062272hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282115
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756308
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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