A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605824



Internal ID16393233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1546603..1563037hg38UCSC Ensembl
Innerchr7:1586239..1602673hg19UCSC Ensembl
Innerchr7:1552765..1569199hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3816435
hg1916435
hg1816435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078363
Samples
Known GenesTMEM184A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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