A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070884



Internal ID19323613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98918332..98942543hg38UCSC Ensembl
chr10:100678089..100702300hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3824212
hg1924212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765832
SamplesKWP1
Known GenesHPSE2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070884
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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