A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609176



Internal ID20982247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94722680..94729136hg38UCSC Ensembl
chr7:94351992..94358448hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg386457
hg196457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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