A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4024912



Internal ID11390276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3406336..3406470hg38UCSC Ensembl
chr19:3406334..3406468hg19UCSC Ensembl
chr19:3357334..3357468hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
hg18135
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1167286
Supporting Variants
SamplesHuRef
Known GenesNFIC
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4024912
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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