A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635248



Internal ID21583553
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 StatusM
Merged Variants
Supporting Variantsnssv17071937
SamplesHG01505
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635248
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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