A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376445



Internal ID21033998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119408663..119409591hg38UCSC Ensembl
chr4:120329818..120330746hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210200
Samples
Known GenesLINC01061
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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