A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602646



Internal ID20975717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2308878..2314269hg38UCSC Ensembl
chr7:2348513..2353904hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg385392
hg195392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154890
Samples
Known GenesSNX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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