A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363670



Internal ID21021223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8872001..9266800hg38UCSC Ensembl
chr4:8873727..9268526hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38394800
hg19394800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214776
Samples
Known GenesLOC650293, USP17L10, USP17L11, USP17L12, USP17L13, USP17L15, USP17L17, USP17L18, USP17L19, USP17L20, USP17L21, USP17L22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363670
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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