A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345127



Internal ID21002680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6749519..6762611hg38UCSC Ensembl
chr2:6889650..6902742hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3813093
hg1913093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090166
Samples
Known GenesLINC00487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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