A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347808



Internal ID21005361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6649516..6652087hg38UCSC Ensembl
chr2:6789648..6792219hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090066
Samples
Known GenesMIR7515
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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