A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403895



Internal ID21061448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141136991..141151762hg38UCSC Ensembl
chr5:140516573..140531343hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3814772
hg1914771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125212
Samples
Known GenesPCDHB5, PCDHB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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