A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131849



Internal ID18934371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97275143..97277642hg38UCSC Ensembl
Outerchr10:99034900..99037399hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv503n106
Supporting Variantsnssv3986427
SamplesKWS1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131849
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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