A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007837



Internal ID19097056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625148..34650948hg38UCSC Ensembl
Innerchr1:35090749..35116549hg19UCSC Ensembl
Innerchr1:34863336..34889136hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3825801
hg1925801
hg1825801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv147n100
Supporting Variantsnssv3463691, nssv3467368, nssv3700641
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007837
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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