A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676401



Internal ID15066367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154095720..154169432hg38UCSC Ensembl
Innerchr1:154068196..154141908hg19UCSC Ensembl
Innerchr1:152334820..152408532hg18UCSC Ensembl
Innerchr1:150881269..150954981hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3873713
hg1973713
hg1873713
hg1773713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520398
Supporting Variants
Samples
Known GenesNUP210L, TPM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676401
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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