A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423004



Internal ID21080557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129791497..129793116hg38UCSC Ensembl
chr7:129431337..129432956hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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