A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3616805



Internal ID12145063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58065665..58065665hg38UCSC Ensembl
chr16:58099569..58099569hg19UCSC Ensembl
chr16:56657070..56657070hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1602811
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3616805
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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