A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381049



Internal ID21038602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94836101..94846400hg38UCSC Ensembl
chr4:95757252..95767551hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214324
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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