A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013788



Internal ID18756320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120147875..120193450hg38UCSC Ensembl
Innerchr3:119866722..119912297hg19UCSC Ensembl
Innerchr3:121349412..121394987hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3845576
hg1945576
hg1845576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604519
Samples
Known GenesGPR156
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013788
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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