A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496821



Internal ID20870024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44200725..44203226hg38UCSC Ensembl
chr17:42278093..42280594hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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