A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318659



Internal ID20851751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20262723..20298207hg38UCSC Ensembl
chr1:20589216..20624700hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3835485
hg1935485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056693
Samples
Known GenesVWA5B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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