A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154929



Internal ID20721969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23535866..23536432hg38UCSC Ensembl
chr7:23575485..23576051hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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