A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495587



Internal ID21153140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67082177..67082597hg38UCSC Ensembl
chr13:67656309..67656729hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012107
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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