A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388127



Internal ID22445997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76288443..76288577hg38UCSC Ensembl
chr17:74284524..74284658hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930754
Supporting Variants
Samples
Known GenesQRICH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388127
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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