A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611122



Internal ID16051845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40845848..40882954hg38UCSC Ensembl
Innerchr8:40703367..40740473hg19UCSC Ensembl
Innerchr8:40822524..40859630hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3837107
hg1937107
hg1837107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156138
Samples1798860372_A
Known GenesZMAT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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