A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968469



Internal ID19228268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103692242..103694442hg38UCSC Ensembl
Outerchr10:105452000..105454200hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121820
Supporting Variants
SamplesKWS2
Known GenesSH3PXD2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968469
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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