A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667728



Internal ID15404380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38744120..38785200hg38UCSC Ensembl
Innerchr21:40116044..40157124hg19UCSC Ensembl
Innerchr21:39037914..39078994hg18UCSC Ensembl
Innerchr21:39037914..39078994hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3841081
hg1941081
hg1841081
hg1741081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516348
Supporting Variants
Samples
Known GenesLINC00114
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667728
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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