A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593770



Internal ID16034493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15982410..15999755hg38UCSC Ensembl
Innerchr4:15984033..16001378hg19UCSC Ensembl
Innerchr4:15593131..15610476hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3817346
hg1917346
hg1817346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153451
Samples1782681275_A
Known GenesPROM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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