A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980718



Internal ID19222873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97208943..97212243hg38UCSC Ensembl
Outerchr10:98968700..98972000hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143513
Supporting Variants
SamplesKWS1
Known GenesARHGAP19-SLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980718
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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