A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069067



Internal ID18971996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97275159..97277660hg38UCSC Ensembl
chr10:99034916..99037417hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771243
SamplesKWP1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069067
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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