A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766551



Internal ID19315589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124504520..124504921hg38UCSC Ensembl
chr9:127266799..127267200hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076204
Supporting Variants
SamplesKWP1
Known GenesNR5A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766551
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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