A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073568



Internal ID18977017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71288596..71289297hg38UCSC Ensembl
chr6:71998299..71999000hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770242
SamplesKWP1
Known GenesOGFRL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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