A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376603



Internal ID22327586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97259546..97286747hg38UCSC Ensembl
chr10:99019303..99046504hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3827202
hg1927202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224713
Supporting Variants
SamplesNA19240
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376603
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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