A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517754



Internal ID15445047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183400103..183407566hg38UCSC Ensembl
Innerchr3:183117891..183125354hg19UCSC Ensembl
Innerchr3:184600585..184608048hg18UCSC Ensembl
Innerchr3:184600593..184608056hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg387464
hg197464
hg187464
hg177464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688593, nssv673682, nssv655864, nssv691389, nssv654592, nssv682453, nssv690553, nssv653122, nssv678370
Samples
Known GenesMCF2L2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517754
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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