A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605445



Internal ID20978516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131788001..131826600hg38UCSC Ensembl
chr6:132109141..132147740hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3838600
hg1938600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6402n223
Supporting Variantsnssv18215567
Samples
Known GenesENPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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