A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577684



Internal ID16365093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76458045..76484662hg38UCSC Ensembl
Innerchr18:74170001..74196618hg19UCSC Ensembl
Innerchr18:72298989..72325606hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3826618
hg1926618
hg1826618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150636
Samples1780862586_A
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577684
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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