A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892862



Internal ID15840132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3937430..3938509hg38UCSC Ensembl
Innerchr19:3937428..3938507hg19UCSC Ensembl
Innerchr19:3888428..3889507hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381080
hg191080
hg181080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578432
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)nssv892862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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