A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769574



Internal ID19314861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66979141..67043742hg38UCSC Ensembl
chr9:40649099..40713700hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3864602
hg1964602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075620
Supporting Variants
SamplesKWP1
Known GenesSPATA31A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769574
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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