A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439956



Internal ID21097509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30304391..30309807hg38UCSC Ensembl
chr10:30593320..30598736hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg385417
hg195417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981393
Samples
Known GenesMTPAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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