A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425547



Internal ID21083100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145063208..145095862hg38UCSC Ensembl
chr7:144760301..144792955hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3832655
hg1932655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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