A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439277



Internal ID21096830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75395371..75395678hg38UCSC Ensembl
chr10:77155129..77155436hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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