A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010225



Internal ID19099443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72346221hg38UCSC Ensembl
Innerchr1:72749848..72811904hg19UCSC Ensembl
Innerchr1:72522436..72584492hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3862057
hg1962057
hg1862057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv181n100
Supporting Variantsnssv3474908, nssv3464490, nssv3473627, nssv3477562, nssv3465510
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)nsv1010225
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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