A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327785



Internal ID20860927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56673901..56675200hg38UCSC Ensembl
chr1:57139574..57140873hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061732
Samples
Known GenesPRKAA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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