A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021702



Internal ID19110920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94543826..94576966hg38UCSC Ensembl
Innerchr8:95556054..95589194hg19UCSC Ensembl
Innerchr8:95625230..95658370hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833141
hg1933141
hg1833141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7273n100
Supporting Variantsnssv3689731
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)nsv1021702
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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