A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074369



Internal ID18974559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4775365..4777266hg38UCSC Ensembl
chr6:4775599..4777500hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769431
SamplesKWP1
Known GenesCDYL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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