A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346965



Internal ID21004518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77342573..77480621hg38UCSC Ensembl
chr2:77569699..77707747hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38138049
hg19138049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207669
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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