A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369004



Internal ID21026557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61612806..61705175hg38UCSC Ensembl
chr3:61598480..61690849hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3892370
hg1992370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212923
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369004
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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