A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118933



Internal ID21421090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38207570..38207570hg38UCSC Ensembl
chr21:39579664..39579664hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666872
Supporting Variants
SamplesHG00731
Known GenesDSCR10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118933
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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