A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1647895



Internal ID12464328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327901..1327901hg38UCSC Ensembl
chr10:1370096..1370096hg19UCSC Ensembl
chr10:1360096..1360096hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3890
hg1990
hg1890
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4089238
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1647895
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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