A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004538



Internal ID16950804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:2591316..2591735hg38UCSC Ensembl
Outerchr3:2633000..2633419hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956822
Supporting Variants
SamplesBILGI_BIOE
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004538
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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