A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763577



Internal ID18963171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97265106..97267640hg38UCSC Ensembl
chr10:99024863..99027397hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069066
Supporting Variants
SamplesKWP1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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