A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950297



Internal ID16952484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:195093272..195098871hg38UCSC Ensembl
Outerchr3:194814001..194819600hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996589
SamplesBILGI_BIOE
Known GenesXXYLT1, XXYLT1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950297
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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