A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763092



Internal ID19306008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95289942..95292243hg38UCSC Ensembl
chr10:97049699..97052000hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069957
Supporting Variants
SamplesKWP1
Known GenesPDLIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763092
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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