A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323982



Internal ID20857105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51587183..51596040hg38UCSC Ensembl
chr1:52052855..52061712hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg388858
hg198858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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