A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607383



Internal ID20980454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115618150..115638391hg38UCSC Ensembl
chr7:115258204..115278445hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3820242
hg1920242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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