A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277393



Internal ID22122009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97259546..97286747hg38UCSC Ensembl
Outerchr10:99019303..99046504hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3827202
hg1927202
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215221
Supporting Variants
SamplesHG00512
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277393
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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