A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764972



Internal ID19313809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67685565..67701988hg38UCSC Ensembl
chr9:46351399..46367500hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816424
hg1916102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075228
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764972
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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