A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473773



Internal ID22531667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41143905..41169319hg38UCSC Ensembl
chr17:39300157..39325571hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3825415
hg1925415
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869299
Supporting Variants
Samples
Known GenesKRTAP4-3, KRTAP4-4, KRTAP4-5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473773
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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