A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504033



Internal ID22561976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16132208..16134407hg38UCSC Ensembl
chr7:16171833..16174032hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846169
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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