A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602500



Internal ID21551158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88831558..88831629hg38UCSC Ensembl
chr16:88897966..88898037hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099573
SamplesNA12878
Known GenesGALNS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602500
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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