A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606746



Internal ID16047469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44104727..44110013hg38UCSC Ensembl
Innerchr7:44144326..44149612hg19UCSC Ensembl
Innerchr7:44110851..44116137hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg385287
hg195287
hg185287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083225
Samples
Known GenesAEBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606746
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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