A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598957



Internal ID16039680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95620562..95621127hg38UCSC Ensembl
Innerchr5:94956266..94956831hg19UCSC Ensembl
Innerchr5:94982022..94982587hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38566
hg19566
hg18566
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038107, nssv1038104, nssv1038103, nssv1038106, nssv1038102, nssv1038101, nssv1038105
Samples
Known GenesGPR150
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598957
Frequency
Sample Size17421
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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