A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765470



Internal ID19305098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29298778..29299279hg38UCSC Ensembl
chr21:30671099..30671600hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072596
Supporting Variants
SamplesKWP1
Known GenesBACH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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