A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009529



Internal ID19098747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184694764..184762081hg38UCSC Ensembl
Innerchr1:184663898..184731215hg19UCSC Ensembl
Innerchr1:182930521..182997838hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3867318
hg1967318
hg1867318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487288
Samples
Known GenesEDEM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009529
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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