A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707728



Internal ID19006009
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 StatusS
Merged Variantsnsv1043897
Supporting Variants
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)nssv3707728
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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