A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578197



Internal ID16018920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049519..1049777hg38UCSC Ensembl
Innerchr19:1049518..1049776hg19UCSC Ensembl
Innerchr19:1000518..1000776hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6182n54
Supporting Variantsnssv891362, nssv891375, nssv891372, nssv891365, nssv891361, nssv891367, nssv891371, nssv891359, nssv891366, nssv891373, nssv891360, nssv891369, nssv891370, nssv891363, nssv891368, nssv891374, nssv891364
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578197
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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