A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997527



Internal ID18810377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269902..25334998hg38UCSC Ensembl
Innerchr1:25596393..25661489hg19UCSC Ensembl
Innerchr1:25468980..25534076hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3865097
hg1965097
hg1865097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n100
Supporting Variantsnssv3463785
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)nsv997527
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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