A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3612703



Internal ID18564298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172746210..172823340hg38UCSC Ensembl
Innerchr3:172464000..172541130hg19UCSC Ensembl
Innerchr3:173946694..174023824hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3877131
hg1977131
hg1877131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000288
Supporting Variants
Samples
Known GenesECT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3612703
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