A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950466



Internal ID17299340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:71747298..71752997hg38UCSC Ensembl
Outerchr6:72457001..72462700hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997477
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950466
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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