A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv956720



Internal ID16250676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38103516..38107960hg38UCSC Ensembl
Innerchr22:38499523..38503967hg19UCSC Ensembl
Innerchr22:36829469..36833913hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384445
hg194445
hg184445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589008
Supporting Variants
Samples
Known GenesBAIAP2L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv956720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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