A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327383



Internal ID20860521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51061469..51061987hg38UCSC Ensembl
chr1:51527141..51527659hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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