A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610512



Internal ID20983583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23006901..23009100hg38UCSC Ensembl
chr7:23046520..23048719hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154880
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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