A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956325



Internal ID16958513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:64628..67992hg38UCSC Ensembl
Outerchr4:64520..67884hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383365
hg193365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004714
SamplesBILGI_BIOE
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956325
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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