A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507723



Internal ID20881017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40410818..40411313hg38UCSC Ensembl
chr15:40703017..40703512hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024196
Samples
Known GenesIVD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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