A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527632



Internal ID20900993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76319078..76319556hg38UCSC Ensembl
chr17:74315159..74315637hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038216
Samples
Known GenesPRPSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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