A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503846



Internal ID22561788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115294670..115297095hg38UCSC Ensembl
chr7:114934724..114937149hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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