A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033318



Internal ID19122540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94543826..94564110hg38UCSC Ensembl
Innerchr8:95556054..95576338hg19UCSC Ensembl
Innerchr8:95625230..95645514hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3820285
hg1920285
hg1820285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7272n100
Supporting Variantsnssv3757324
Samples
Known GenesKIAA1429
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033318
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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