A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704831



Internal ID19003112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:181881002..181927264hg38UCSC Ensembl
Innerchr1:181850137..181896399hg19UCSC Ensembl
Innerchr1:180116760..180163022hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3846263
hg1946263
hg1846263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006813
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3704831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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