A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504709



Internal ID22562652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19878413..19891990hg38UCSC Ensembl
chr7:19918036..19931613hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813578
hg1913578
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504709
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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