A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419860



Internal ID21077413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132054517..132065991hg38UCSC Ensembl
chr7:131739276..131750750hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3811475
hg1911475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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