A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3467118



Internal ID18715451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25320483hg38UCSC Ensembl
Innerchr1:25595935..25646974hg19UCSC Ensembl
Innerchr1:25468522..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851040
hg1951040
hg1851040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007934
Supporting Variants
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)nssv3467118
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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