A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043897



Internal ID19133116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24234860..24256504hg38UCSC Ensembl
Innerchr10:24523789..24545433hg19UCSC Ensembl
Innerchr10:24563795..24585439hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3821645
hg1921645
hg1821645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520764, nssv3512279, nssv3514091, nssv3707727, nssv3707728
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043897
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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