A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506977



Internal ID20880265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56382401..56396700hg38UCSC Ensembl
chr15:56674599..56688898hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024900
Samples
Known GenesTEX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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