A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619920



Internal ID20992991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42837390..42841495hg38UCSC Ensembl
chr7:42876989..42881094hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384106
hg194106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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