A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952405



Internal ID17301279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:5295202..5296201hg38UCSC Ensembl
Outerchr18:5295201..5296200hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998838
SamplesBILGI_BIOE
Known GenesZBTB14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952405
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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