A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501958



Internal ID18800239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212744189..212774179hg38UCSC Ensembl
Innerchr1:212917531..212947521hg19UCSC Ensembl
Innerchr1:210984154..211014144hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3829991
hg1929991
hg1829991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005983
Supporting Variants
Samples
Known GenesNSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501958
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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