A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501916



Internal ID22559855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69157801..69158800hg38UCSC Ensembl
chr7:68622788..68623787hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501916
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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