A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500088



Internal ID22558024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103625656..103627790hg38UCSC Ensembl
chr7:103266103..103268237hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860575
Supporting Variants
Samples
Known GenesRELN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500088
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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