A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614307



Internal ID20987378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99079127..99080701hg38UCSC Ensembl
chr7:98676750..98678324hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161317
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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