A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505386



Internal ID22563330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2921081..2936892hg38UCSC Ensembl
chr7:2960715..2976526hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3815812
hg1915812
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846217
Supporting Variants
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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