A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328991



Internal ID20862141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195922539..196014612hg38UCSC Ensembl
chr1:195891669..195983742hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3892074
hg1992074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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