A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069477



Internal ID18978677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46377822..46397534hg38UCSC Ensembl
chr10:47748999..47768800hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819713
hg1919802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771464
SamplesKWP1
Known GenesANXA8L1, ANXA8L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069477
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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