A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329636



Internal ID20862789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189253878..189578778hg38UCSC Ensembl
chr1:189223009..189547908hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38324901
hg19324900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv473n223
Supporting Variantsnssv18054989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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