A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008571



Internal ID18751102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25275356..25336807hg38UCSC Ensembl
Innerchr1:25601847..25663298hg19UCSC Ensembl
Innerchr1:25474434..25535885hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3861452
hg1961452
hg1861452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n100
Supporting Variantsnssv3472884, nssv3477985, nssv3480916, nssv3700630
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008571
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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