A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340581



Internal ID20998134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5972692..5974581hg38UCSC Ensembl
chr2:6112824..6114713hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088785
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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