A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452728



Internal ID21110281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71882600..71887425hg38UCSC Ensembl
chr10:73642358..73647183hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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