A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1044797



Internal ID11861236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56444724..56444724hg38UCSC Ensembl
chr19:56956093..56956093hg19UCSC Ensembl
chr19:61647905..61647905hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38336
hg19336
hg18336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3862468
SamplesHuRef
Known GenesZNF667
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1044797
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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