A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578201



Internal ID16018924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049519..1049989hg38UCSC Ensembl
Innerchr19:1049518..1049988hg19UCSC Ensembl
Innerchr19:1000518..1000988hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38471
hg19471
hg18471
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6180n54
Supporting Variantsnssv891413, nssv891424, nssv891420, nssv891406, nssv891403, nssv891415, nssv891414, nssv891410, nssv891407, nssv891421, nssv891425, nssv891419, nssv891405, nssv891423, nssv891409, nssv891404, nssv891416, nssv891422, nssv891417, nssv891411, nssv891408, nssv891418, nssv891412
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578201
Frequency
Sample Size17421
Observed Gain8
Observed Loss15
Observed Complex0
Frequencyn/a


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