A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069500



Internal ID19322655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78973642..78974443hg38UCSC Ensembl
chr10:80733399..80734200hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766320
SamplesKWP1
Known GenesZMIZ1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069500
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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