A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706027



Internal ID15442679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10065707..10179139hg38UCSC Ensembl
Innerchr1:10125765..10239197hg19UCSC Ensembl
Innerchr1:10048352..10161784hg18UCSC Ensembl
Innerchr1:10060031..10173463hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38113433
hg19113433
hg18113433
hg17113433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522629
Supporting Variants
Samples
Known GenesUBE4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706027
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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