A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531894



Internal ID20905255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76314401..76333182hg38UCSC Ensembl
chr17:74310482..74329263hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3818782
hg1918782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038215
Samples
Known GenesPRPSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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