A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772877



Internal ID18960471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:974599..977600hg38UCSC Ensembl
chr9:974599..977600hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075185
Supporting Variants
SamplesKWP1
Known GenesDMRT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772877
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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