A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069462



Internal ID19326001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21534070..21535071hg38UCSC Ensembl
chr10:21822999..21824000hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764187
SamplesKWP1
Known GenesMLLT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069462
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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