A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980854



Internal ID18861652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:110226442..110227242hg38UCSC Ensembl
Outerchr10:111986200..111987000hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118187
Supporting Variants
SamplesKWS1
Known GenesMXI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980854
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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