A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605875



Internal ID20978946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162062248..162370661hg38UCSC Ensembl
chr6:162483280..162791693hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38308414
hg19308414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6481n223
Supporting Variantsnssv18139247
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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