A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600240



Internal ID20973311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26229303..26235187hg38UCSC Ensembl
chr7:26268923..26274807hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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