A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499852



Internal ID20873077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61917535..61925303hg38UCSC Ensembl
chr16:61951439..61959207hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387769
hg197769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030814
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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