A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996701



Internal ID17289653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38753280..38754579hg38UCSC Ensembl
Outerchr4:38754901..38756200hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950575
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996701
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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