A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544895



Internal ID15985618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:917392..1054900hg38UCSC Ensembl
Innerchr1:852772..990280hg19UCSC Ensembl
Innerchr1:842635..980143hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38137509
hg19137509
hg18137509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv707675
Samples
Known GenesAGRN, C1orf170, HES4, ISG15, KLHL17, LOC100130417, NOC2L, PLEKHN1, SAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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