A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771256



Internal ID18963459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12554276..12554607hg38UCSC Ensembl
chr10:12596275..12596606hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069023
Supporting Variants
SamplesKWP1
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771256
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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