A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523997



Internal ID15104604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136110306..136463173hg38UCSC Ensembl
Innerchr2:136867876..137220743hg19UCSC Ensembl
Innerchr2:136584346..136937213hg18UCSC Ensembl
Innerchr2:136701608..137054475hg17UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38352868
hg19352868
hg18352868
hg17352868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699857
Samples
Known GenesCXCR4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523997
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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