A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515751



Internal ID15096358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3010718..3013563hg38UCSC Ensembl
Innerchr3:3052402..3055247hg19UCSC Ensembl
Innerchr3:3027402..3030247hg18UCSC Ensembl
Innerchr3:3027402..3030247hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg382846
hg192846
hg182846
hg172846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690369, nssv690219, nssv664675, nssv677699
Samples
Known GenesCNTN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515751
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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