A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505385



Internal ID22563329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29015590..29019773hg38UCSC Ensembl
chr7:29055206..29059389hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg384184
hg194184
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846287
Supporting Variants
Samples
Known GenesCPVL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505385
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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