A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504305



Internal ID20877566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40055467..40059170hg38UCSC Ensembl
chr15:40347668..40351371hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383704
hg193704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024506
Samples
Known GenesSRP14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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