A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009060



Internal ID19098278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201469976..201491742hg38UCSC Ensembl
Innerchr1:201439104..201460870hg19UCSC Ensembl
Innerchr1:199705727..199727493hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3821767
hg1921767
hg1821767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502499
Samples
Known GenesCSRP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009060
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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