A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414722



Internal ID21072275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97114990..97115750hg38UCSC Ensembl
chr5:96450694..96451454hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135700
Samples
Known GenesLIX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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