A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076174



Internal ID19324543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67860853..67861654hg38UCSC Ensembl
chr9:67928299..67929100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766832
SamplesKWP1
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076174
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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