A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064535



Internal ID21973768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185399125..185399125hg38UCSC Ensembl
chr4:186320279..186320279hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553907
Samples
Known GenesANKRD37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064535
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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