A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516128



Internal ID15096735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11683432..11695677hg38UCSC Ensembl
Innerchr18:11683431..11695676hg19UCSC Ensembl
Innerchr18:11673431..11685676hg18UCSC Ensembl
Innerchr18:11673431..11685676hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3812246
hg1912246
hg1812246
hg1712246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669192, nssv668546, nssv690798, nssv683589, nssv692491, nssv690447, nssv671148, nssv684569, nssv666392, nssv654726, nssv673586, nssv679994, nssv667147, nssv680483
Samples
Known GenesGNAL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516128
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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