A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350552



Internal ID21008105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6098503..6806437hg38UCSC Ensembl
chr2:6238635..6946568hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38707935
hg19707934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206365
Samples
Known GenesLINC00487, MIR7515
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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