A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630449



Internal ID21822496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7938194..7938287hg38UCSC Ensembl
chr17:7841512..7841605hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038414
Supporting Variants
Samples
Known GenesCNTROB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630449
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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