A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347732



Internal ID21005285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7423109..7430302hg38UCSC Ensembl
chr2:7563240..7570433hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg387194
hg197194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207052
Samples
Known GenesLOC100506274
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347732
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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