A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009705



Internal ID18752236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100621212..100704745hg38UCSC Ensembl
Innerchr3:100340056..100423589hg19UCSC Ensembl
Innerchr3:101822746..101906279hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3883534
hg1983534
hg1883534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4831n100
Supporting Variantsnssv3604241
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)nsv1009705
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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