A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069482



Internal ID19316618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50076639..50100640hg38UCSC Ensembl
chr10:51836399..51860400hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3824002
hg1924002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763847
SamplesKWP1
Known GenesFAM21A, FAM21B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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