A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817753



Internal ID21263091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55120514..55120514hg38UCSC Ensembl
chr8:56033074..56033074hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711242
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817753
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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