A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617543



Internal ID20990614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100399195..100407647hg38UCSC Ensembl
chr7:99996818..100005270hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388453
hg198453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220598
Samples
Known GenesPILRA, ZCWPW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617543
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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