A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011935



Internal ID18754471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8433912..8523307hg38UCSC Ensembl
Innerchr3:8475598..8564993hg19UCSC Ensembl
Innerchr3:8450598..8539993hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3889396
hg1989396
hg1889396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591845
Samples
Known GenesLMCD1, LMCD1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011935
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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