A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104789



Internal ID21487705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37698149..37699470hg38UCSC Ensembl
chr19:38189050..38190371hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381322
hg191322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602433
Supporting Variants
SamplesNA18534
Known GenesZNF607
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104789
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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