A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004709



Internal ID16950975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112548833..112549123hg38UCSC Ensembl
Outerchr4:113469989..113470279hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956315
Supporting Variants
SamplesBILGI_BIOE
Known GenesC4orf21
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004709
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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