A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337705



Internal ID20995258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167056875..167057326hg38UCSC Ensembl
chr2:167913385..167913836hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080278
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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