A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326572



Internal ID20859709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77922272..77922811hg38UCSC Ensembl
chr1:78387957..78388496hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063234
Samples
Known GenesNEXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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