A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007914



Internal ID19097133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:235813294..235881466hg38UCSC Ensembl
Innerchr1:235976594..236044766hg19UCSC Ensembl
Innerchr1:234043217..234111389hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3868173
hg1968173
hg1868173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv588n100
Supporting Variantsnssv3494674
Samples
Known GenesLYST, MIR1537
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007914
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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