A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377871



Internal ID21035424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139324135..139397409hg38UCSC Ensembl
chr4:140245289..140318563hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3873275
hg1973275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213038
Samples
Known GenesNAA15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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