A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007850



Internal ID19097069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1696467..1756199hg38UCSC Ensembl
Innerchr1:1627906..1687638hg19UCSC Ensembl
Innerchr1:1617766..1677498hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3859733
hg1959733
hg1859733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n100
Supporting Variantsnssv3476085
Samples
Known GenesCDK11A, CDK11B, MMP23A, NADK, SLC35E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007850
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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