A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503811



Internal ID22561752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110790722..110792421hg38UCSC Ensembl
chr7:110430778..110432477hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863508
Supporting Variants
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503811
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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