A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982813



Internal ID19206775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132007664..132014959hg38UCSC Ensembl
Outerchr10:133821168..133828463hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg387296
hg197296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119852
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982813
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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