A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762655



Internal ID19315152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143536862..143537263hg38UCSC Ensembl
chr6:143857999..143858400hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074965
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762655
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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