A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607314



Internal ID20980385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96563701..96564400hg38UCSC Ensembl
chr6:97011577..97012276hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150483
Samples
Known GenesFHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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