A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515496



Internal ID20888856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75010269..75018894hg38UCSC Ensembl
chr16:75044167..75052792hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg388626
hg198626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031454
Samples
Known GenesZNRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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