A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442663



Internal ID22500533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52876956..52881062hg38UCSC Ensembl
chr6:52741754..52745860hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg384107
hg194107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442663
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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