A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388532



Internal ID21046085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118561301..118651900hg38UCSC Ensembl
chr4:119482456..119573055hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3890600
hg1990600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5432n223
Supporting Variantsnssv18211957
Samples
Known GenesLOC729218
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388532
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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