A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577260



Internal ID16017983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66545786..66553653hg38UCSC Ensembl
Innerchr18:64213023..64220890hg19UCSC Ensembl
Innerchr18:62364003..62371870hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg387868
hg197868
hg187868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886019
Samples
Known GenesCDH19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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