A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008381



Internal ID19097599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:150748778..150773082hg38UCSC Ensembl
Innerchr1:150721254..150745558hg19UCSC Ensembl
Innerchr1:148987878..149012182hg18UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3824305
hg1924305
hg1824305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3495939
Samples
Known GenesCTSS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008381
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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