A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074003



Internal ID18973478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104774144..104774394hg38UCSC Ensembl
chr6:105222019..105222269hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764966
SamplesKWP1
Known GenesHACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074003
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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