A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503551



Internal ID22561492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85444853..85452689hg38UCSC Ensembl
chr7:85074169..85082005hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387837
hg197837
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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