A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074441



Internal ID18970824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160005567..160006268hg38UCSC Ensembl
chr6:160426599..160427300hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763732
SamplesKWP1
Known GenesAIRN, IGF2R
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074441
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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