A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996224



Internal ID15235084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8771366..8892364hg38UCSC Ensembl
Innerchr19:8882042..9003040hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38120999
hg19120999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483078
Supporting Variants
Samples
Known GenesMBD3L1, MUC16, ZNF558
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996224
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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