A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500649



Internal ID22558586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108954403..109003550hg38UCSC Ensembl
chr7:108594460..108643607hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3849148
hg1949148
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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