A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075695



Internal ID18978619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136675307..136675570hg38UCSC Ensembl
chr9:139569759..139570022hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769291
SamplesKWP1
Known GenesAGPAT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075695
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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