A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448520



Internal ID22506390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63643314..63643371hg38UCSC Ensembl
chr6:64353219..64353276hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897476
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448520
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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