A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330176



Internal ID20863331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28853901..28854813hg38UCSC Ensembl
chr1:29180413..29181325hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059988
Samples
Known GenesOPRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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