A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068307



Internal ID18979770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44927780..44928730hg38UCSC Ensembl
chr10:45423228..45424178hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770218
SamplesKWP1
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068307
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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