A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326512



Internal ID20859648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38967340..38975198hg38UCSC Ensembl
chr1:39433012..39440870hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387859
hg197859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv161n223
Supporting Variantsnssv18060079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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