A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954568



Internal ID17303442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:4138928..4139257hg38UCSC Ensembl
Outerchr17:4042222..4042551hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001583
SamplesBILGI_BIOE
Known GenesZZEF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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