A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074381



Internal ID18975393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13485767..13486568hg38UCSC Ensembl
chr6:13485999..13486800hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771229
SamplesKWP1
Known GenesGFOD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074381
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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