A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427416



Internal ID21084969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55135656..55135927hg38UCSC Ensembl
chr8:56048216..56048487hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169109
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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