A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607518



Internal ID20980589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106550659..106554744hg38UCSC Ensembl
chr7:106191105..106195190hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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