A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767811



Internal ID19309539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34073199..34074400hg38UCSC Ensembl
chr21:35445499..35446700hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073127
Supporting Variants
SamplesKWP1
Known GenesMRPS6, SLC5A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767811
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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