A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502069



Internal ID22560009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140075515..140079718hg38UCSC Ensembl
chr7:139775315..139779518hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384204
hg194204
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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