A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006559



Internal ID18749090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100605431..100709093hg38UCSC Ensembl
Innerchr3:100324275..100427937hg19UCSC Ensembl
Innerchr3:101806965..101910627hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38103663
hg19103663
hg18103663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4830n100
Supporting Variantsnssv3604233, nssv3735191
Samples
Known GenesGPR128
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006559
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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