A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557356



Internal ID15998079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9190990..9210335hg38UCSC Ensembl
Innerchr12:9343586..9362931hg19UCSC Ensembl
Innerchr12:9234853..9254198hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3819346
hg1919346
hg1819346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175823
Samples1780862528_A
Known GenesPZP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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