A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770598



Internal ID19305264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40861871..40910315hg38UCSC Ensembl
chr9:66814899..66863400hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3848445
hg1948502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076668
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770598
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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