A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014835



Internal ID18757370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25244339..25292537hg38UCSC Ensembl
Innerchr1:25570830..25619028hg19UCSC Ensembl
Innerchr1:25443417..25491615hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3848199
hg1948199
hg1848199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv135n100
Supporting Variantsnssv3478484
Samples
Known GenesC1orf63, RHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014835
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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