A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510254



Internal ID22568204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94156403..94160002hg38UCSC Ensembl
chr8:95168631..95172230hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862542
Supporting Variants
Samples
Known GenesCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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