A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892833



Internal ID15840103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3937165..3938033hg38UCSC Ensembl
Innerchr19:3937163..3938031hg19UCSC Ensembl
Innerchr19:3888163..3889031hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38869
hg19869
hg18869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578424
Supporting Variants
Samples
Known GenesNMRK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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