A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980851



Internal ID18872932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102643143..102644943hg38UCSC Ensembl
Outerchr10:104402900..104404700hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118184
Supporting Variants
SamplesKWS1
Known GenesTRIM8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980851
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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