A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130299



Internal ID18918141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97275106..97277640hg38UCSC Ensembl
Outerchr10:99034863..99037397hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv503n106
Supporting Variantsnssv3988414, nssv3964320
SamplesKWS2, KWS1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130299
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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