A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026768



Internal ID19115986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94543826..94557338hg38UCSC Ensembl
Innerchr8:95556054..95569566hg19UCSC Ensembl
Innerchr8:95625230..95638742hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3813513
hg1913513
hg1813513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7271n100
Supporting Variantsnssv3689728
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)nsv1026768
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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