A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605586



Internal ID20978657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101703471..101752339hg38UCSC Ensembl
chr6:102151346..102200214hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3848869
hg1948869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134549
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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