A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438482



Internal ID21096035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132629507..132629843hg38UCSC Ensembl
chr10:134443011..134443347hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978559
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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