A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507150



Internal ID22565098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50459959..50461058hg38UCSC Ensembl
chr7:50527657..50528756hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846715
Supporting Variants
Samples
Known GenesDDC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507150
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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