A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061484



Internal ID21970717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185240842..185240842hg38UCSC Ensembl
chr4:186161996..186161996hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546870
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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