A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601763



Internal ID20974834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8843748..9115815hg38UCSC Ensembl
chr7:8883378..9155445hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38272068
hg19272068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6574n223
Supporting Variantsnssv18161953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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