A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517527



Internal ID15444820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:5917188..5926142hg38UCSC Ensembl
Innerchr12:6026354..6035308hg19UCSC Ensembl
Innerchr12:5896615..5905569hg18UCSC Ensembl
Innerchr12:5896615..5905569hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg388955
hg198955
hg188955
hg178955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666095, nssv665579, nssv666510, nssv687929, nssv652278
Samples
Known GenesANO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517527
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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