A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355989



Internal ID21013542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100657601..100726300hg38UCSC Ensembl
chr3:100376445..100445144hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3868700
hg1968700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4954n223
Supporting Variantsnssv18208864
Samples
Known GenesGPR128, TFG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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