A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510297



Internal ID20883614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30876378..30889878hg38UCSC Ensembl
chr16:30887699..30901199hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3813501
hg1913501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029195
Samples
Known GenesBCL7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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