A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547530



Internal ID20920731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14515137..14515501hg38UCSC Ensembl
chr21:15887458..15887822hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068631
Samples
Known GenesSAMSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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