A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934561



Internal ID22709889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75111633..75112142hg38UCSC Ensembl
chr17:73107728..73108237hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383823
Samples
Known GenesARMC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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