A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080028



Internal ID21457911
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 StatusS
Merged Variantsnsv5601556
Supporting Variants
SamplesHG02587
Known GenesLOC440354, LOC595101
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080028
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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