A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502621



Internal ID18800902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169238702..169301757hg38UCSC Ensembl
Innerchr1:169207940..169270995hg19UCSC Ensembl
Innerchr1:167474564..167537619hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3863056
hg1963056
hg1863056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009170
Supporting Variants
Samples
Known GenesNME7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502621
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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