A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045300



Internal ID19134519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24088733..24099347hg38UCSC Ensembl
Innerchr10:24377662..24388276hg19UCSC Ensembl
Innerchr10:24417668..24428282hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810615
hg1910615
hg1810615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv692n100
Supporting Variantsnssv3506448, nssv3504552, nssv3510636, nssv3516765, nssv3505250
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)nsv1045300
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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