A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1695561



Internal ID12858679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55361620..55361797hg38UCSC Ensembl
chr19:55872988..55873165hg19UCSC Ensembl
chr19:60564800..60564977hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38178
hg19178
hg18178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3762575
SamplesHuRef
Known GenesFAM71E2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1695561
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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