A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695198



Internal ID15085164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5679690..5726530hg38UCSC Ensembl
Innerchr10:5721653..5768493hg19UCSC Ensembl
Innerchr10:5761659..5808499hg18UCSC Ensembl
Innerchr10:5761659..5808499hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3846841
hg1946841
hg1846841
hg1746841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522415
Supporting Variants
Samples
Known GenesFAM208B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695198
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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