A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069861



Internal ID19316165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11108479..11108909hg38UCSC Ensembl
chr2:11248605..11249035hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767095
SamplesKWP1
Known GenesFLJ33534
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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