A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602383



Internal ID20975454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24027642..24028371hg38UCSC Ensembl
chr7:24067261..24067990hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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