A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074037



Internal ID18976278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167826519..167827720hg38UCSC Ensembl
chr6:168227199..168228400hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764709
SamplesKWP1
Known GenesMLLT4, MLLT4-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074037
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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