A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999026



Internal ID19158562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208265627..208284977hg38UCSC Ensembl
Innerchr1:208438972..208458322hg19UCSC Ensembl
Innerchr1:206505595..206524945hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3819351
hg1919351
hg1819351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv566n100
Supporting Variantsnssv3499774
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999026
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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