A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523958



Internal ID15104565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9150844..9396476hg38UCSC Ensembl
Innerchr12:9303440..9549072hg19UCSC Ensembl
Innerchr12:9194707..9440339hg18UCSC Ensembl
Innerchr12:9194707..9440339hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38245633
hg19245633
hg18245633
hg17245633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699808
Samples
Known GenesA2MP1, LINC00987, LOC642846, MIR1244-1, MIR1244-2, MIR1244-3, PZP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523958
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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