A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477954



Internal ID22535855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51709888..51720871hg38UCSC Ensembl
chr19:52213141..52224124hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3810984
hg1910984
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869023
Supporting Variants
Samples
Known GenesHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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