A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075185



Internal ID18972762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:974599..977600hg38UCSC Ensembl
chr9:974599..977600hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772877
SamplesKWP1
Known GenesDMRT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075185
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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