A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893562



Internal ID15840832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11931134..11934386hg38UCSC Ensembl
Innerchr19:12041949..12045201hg19UCSC Ensembl
Innerchr19:11902949..11906201hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383253
hg193253
hg183253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578624
Supporting Variants
Samples
Known GenesZNF700
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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