A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417170



Internal ID21074723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50228301..50229700hg38UCSC Ensembl
chr8:51140861..51142260hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7334n223
Supporting Variantsnssv18168530
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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