A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608155



Internal ID16048878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111082426..111711456hg38UCSC Ensembl
Innerchr7:110722482..111351512hg19UCSC Ensembl
Innerchr7:110509718..111138748hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38629031
hg19629031
hg18629031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092688
Samples
Known GenesIMMP2L, LRRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608155
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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