A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143496



Internal ID18902030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26710071..26713271hg38UCSC Ensembl
Outerchr10:26999000..27002200hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv382n106
Supporting Variantsnssv3980701
SamplesKWS1
Known GenesPDSS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143496
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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