A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008109



Internal ID19097328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106802169..106835738hg38UCSC Ensembl
Innerchr1:107344791..107378360hg19UCSC Ensembl
Innerchr1:107146314..107179883hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3833570
hg1933570
hg1833570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494890
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)nsv1008109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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