A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076868



Internal ID21986101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94976865..94976865hg38UCSC Ensembl
chr4:95898016..95898016hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541744
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076868
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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