A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605212



Internal ID20978283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83120101..83127000hg38UCSC Ensembl
chr7:82749417..82756316hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221138
Samples
Known GenesPCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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