A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771128



Internal ID18965034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28299670..28303871hg38UCSC Ensembl
chr10:28588599..28592800hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384202
hg194202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069035
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771128
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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