A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956508



Internal ID16958695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136278755..136279685hg38UCSC Ensembl
Outerchr6:136599893..136600823hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003417
SamplesBILGI_BIOE
Known GenesBCLAF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956508
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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