A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332688



Internal ID20865862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32935375..32935985hg38UCSC Ensembl
chr1:33400976..33401586hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060945, nssv18203616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332688
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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