A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771093



Internal ID19315077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4894877..4894965hg38UCSC Ensembl
chr6:4895111..4895199hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074370
Supporting Variants
SamplesKWP1
Known GenesCDYL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771093
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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