A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615872



Internal ID20988943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1752322..1784157hg38UCSC Ensembl
chr7:1791958..1823793hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831836
hg1931836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6538n223
Supporting Variantsnssv18152978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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