A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372551



Internal ID21030104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108878179..109297541hg38UCSC Ensembl
chr3:108597026..109016388hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38419363
hg19419363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4974n223
Supporting Variantsnssv18207217
Samples
Known GenesDPPA2, FLJ22763, GUCA1C, LINC00488, MORC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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