A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972405



Internal ID16266361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126296824..126330591hg38UCSC Ensembl
Innerchr3:126015667..126049434hg19UCSC Ensembl
Innerchr3:127498357..127532124hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3833768
hg1933768
hg1833768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591499
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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