A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045509



Internal ID18788040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126162634..127193365hg38UCSC Ensembl
Innerchr10:127851203..128991629hg19UCSC Ensembl
Innerchr10:127841193..128881619hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381030732
hg191140427
hg181040427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516050, nssv3513346
Samples
Known GenesADAM12, C10orf90, DOCK1, FAM196A, LINC00601
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045509
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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