A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071937



Internal ID21451247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97251740..97251740hg38UCSC Ensembl
chr10:99011497..99011497hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635248
Supporting Variants
SamplesHG01505
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071937
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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