A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156988



Internal ID20724028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21710038..21710569hg38UCSC Ensembl
chr7:21749656..21750187hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606323
Supporting Variants
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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