A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437136



Internal ID21094689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59878260..59879328hg38UCSC Ensembl
chr10:61638018..61639086hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982670
Samples
Known GenesCCDC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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