A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329984



Internal ID20863138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163566600..163813144hg38UCSC Ensembl
chr1:163536390..163782381hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38246545
hg19245992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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