A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035124



Internal ID20602164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35596501..35597200hg38UCSC Ensembl
chr17:33923520..33924219hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505189
Supporting Variants
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00462


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