A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498031



Internal ID20871239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3121759..3139996hg38UCSC Ensembl
chr16:3171760..3189997hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3818238
hg1918238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028939
Samples
Known GenesZNF213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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