A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577687



Internal ID16365096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76484662..76521109hg38UCSC Ensembl
Innerchr18:74196618..74233066hg19UCSC Ensembl
Innerchr18:72325606..72362054hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3836448
hg1936449
hg1836449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6076n54
Supporting Variantsnssv1150638
SamplesNINDS_273
Known GenesFLJ44313, ZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577687
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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