A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327569



Internal ID20860709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179145993..179146328hg38UCSC Ensembl
chr1:179115128..179115463hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054112
Samples
Known GenesABL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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