A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608666



Internal ID20981737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26612789..26629365hg38UCSC Ensembl
chr7:26652408..26668984hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3816577
hg1916577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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