A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385729



Internal ID22443599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7337591..7339347hg38UCSC Ensembl
chr17:7240910..7242666hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381757
hg191757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932169
Supporting Variants
Samples
Known GenesACAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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