A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076670



Internal ID19325990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67869153..67885754hg38UCSC Ensembl
chr9:67936599..67953200hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3816602
hg1916602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764899
SamplesKWP1
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076670
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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