A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504542



Internal ID22562485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143845328..143853146hg38UCSC Ensembl
chr7:143542421..143550239hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg387819
hg197819
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865950
Supporting Variants
Samples
Known GenesFAM115A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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