A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331330



Internal ID20864493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169201816..169316970hg38UCSC Ensembl
chr1:169171054..169286208hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38115155
hg19115155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053645
Samples
Known GenesNME7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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