A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007364



Internal ID19096583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208248131..208284828hg38UCSC Ensembl
Innerchr1:208421476..208458173hg19UCSC Ensembl
Innerchr1:206488099..206524796hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3836698
hg1936698
hg1836698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv565n100
Supporting Variantsnssv3492634
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)nsv1007364
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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