A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503402



Internal ID22561343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156901371..156907358hg38UCSC Ensembl
chr7:156694065..156700052hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385988
hg195988
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503402
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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