A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007896



Internal ID19097115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208905758..208963474hg38UCSC Ensembl
Innerchr1:209079103..209136819hg19UCSC Ensembl
Innerchr1:207145726..207203442hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3857717
hg1957717
hg1857717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n100
Supporting Variantsnssv3494653
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)nsv1007896
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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