A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601556



Internal ID21550204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30252116..30291508hg38UCSC Ensembl
chr16:30263437..30302829hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3839393
hg1939393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080028
SamplesHG02587
Known GenesLOC440354, LOC595101
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601556
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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