A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069447



Internal ID19325777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5156476..5156527hg38UCSC Ensembl
chr10:5198670..5198731hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3852
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765946
SamplesKWP1
Known GenesAKR1CL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069447
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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