A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011672



Internal ID19100889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256788..25335709hg38UCSC Ensembl
Innerchr1:25583279..25662200hg19UCSC Ensembl
Innerchr1:25455866..25534787hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3878922
hg1978922
hg1878922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv136n100
Supporting Variantsnssv3471685
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)nsv1011672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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