A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012224



Internal ID19101442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113853968..113904192hg38UCSC Ensembl
Innerchr3:113572815..113623039hg19UCSC Ensembl
Innerchr3:115055505..115105729hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3850225
hg1950225
hg1850225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4841n100
Supporting Variantsnssv3604464
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)nsv1012224
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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