A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005582



Internal ID19094799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40877389..40921331hg38UCSC Ensembl
Innerchr1:41343061..41387003hg19UCSC Ensembl
Innerchr1:41115648..41159590hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3843943
hg1943943
hg1843943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155n100
Supporting Variantsnssv3473800
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)nsv1005582
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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