A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012955



Internal ID19102172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113845386..113895642hg38UCSC Ensembl
Innerchr3:113564233..113614489hg19UCSC Ensembl
Innerchr3:115046923..115097179hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3850257
hg1950257
hg1850257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4841n100
Supporting Variantsnssv3604449, nssv3604448
Samples
Known GenesGRAMD1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012955
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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