A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439326



Internal ID21096879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30667448..30668197hg38UCSC Ensembl
chr10:30956377..30957126hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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