A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391017



Internal ID21048570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96994886..97090117hg38UCSC Ensembl
chr4:97916037..98011268hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3895232
hg1995232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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