A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076685



Internal ID19325320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68220583..68226784hg38UCSC Ensembl
chr9:70835499..70841700hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg386202
hg196202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770886
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076685
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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