A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955809



Internal ID16957996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24811662..24817718hg38UCSC Ensembl
Outerchr6:24811890..24817946hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386057
hg196057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003383
SamplesBILGI_BIOE
Known GenesFAM65B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955809
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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