A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316255



Internal ID20849333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27263..377948hg38UCSC Ensembl
chr2:27263..377948hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38350686
hg19350686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209138
Samples
Known GenesACP1, FAM110C, FAM150B, SH3YL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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