A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005265



Internal ID17298217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:37037005..37037217hg38UCSC Ensembl
Outerchr4:37038627..37038839hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956880
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005265
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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