A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415586



Internal ID21073139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140828420..140848787hg38UCSC Ensembl
chr5:140208005..140228372hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3820368
hg1920368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125179
Samples
Known GenesPCDHA1, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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