A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154953



Internal ID20721993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23933301..23938700hg38UCSC Ensembl
chr7:23972920..23978319hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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