A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996056



Internal ID18844654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97275129..97277641hg38UCSC Ensembl
Outerchr10:99034886..99037398hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382513
hg192513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150585
Supporting Variants
SamplesKWB1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996056
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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