A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569801



Internal ID16357210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67576449..67576686hg38UCSC Ensembl
Innerchr15:67868787..67869024hg19UCSC Ensembl
Innerchr15:65655841..65656078hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38238
hg19238
hg18238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844334, nssv844356, nssv844350, nssv844348, nssv844336, nssv844352, nssv844347, nssv844349, nssv844330, nssv844360, nssv844357, nssv844345, nssv844346, nssv844337, nssv844342, nssv844338, nssv844354, nssv844328, nssv844329, nssv844339, nssv844343, nssv844333, nssv844351, nssv844353, nssv844341, nssv844361, nssv844326, nssv844327, nssv844332, nssv844325, nssv844324, nssv844344, nssv844358, nssv844355, nssv844340, nssv844359, nssv844335, nssv844331
Samples
Known GenesMAP2K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569801
Frequency
Sample Size17421
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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