A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601513



Internal ID20974584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115282634..115283419hg38UCSC Ensembl
chr7:114922688..114923473hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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