A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004124



Internal ID18746655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158428926..159090849hg38UCSC Ensembl
Innerchr3:158146715..158808638hg19UCSC Ensembl
Innerchr3:159629409..160291332hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38661924
hg19661924
hg18661924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606388
Samples
Known GenesGFM1, IQCJ, IQCJ-SCHIP1, LOC100996447, LXN, MFSD1, MLF1, RARRES1, RSRC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004124
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer