A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765587



Internal ID18958602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127118454..127118755hg38UCSC Ensembl
chr6:127439599..127439900hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074961
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765587
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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