A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955815



Internal ID17304688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152708861..152712650hg38UCSC Ensembl
Outerchr6:153029996..153033785hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003389
SamplesBILGI_BIOE
Known GenesMYCT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955815
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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