A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601285



Internal ID20974356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68248691..68257667hg38UCSC Ensembl
chr7:67713678..67722654hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg388977
hg198977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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