A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425501



Internal ID22483371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167004613..167004681hg38UCSC Ensembl
chr6:167418101..167418169hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917517
Supporting Variants
Samples
Known GenesFGFR1OP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425501
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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