A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770971



Internal ID18962669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135714453..135714854hg38UCSC Ensembl
chr9:138606299..138606700hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075690
Supporting Variants
SamplesKWP1
Known GenesKCNT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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