A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439439



Internal ID21096992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29711137..29712914hg38UCSC Ensembl
chr10:30000066..30001843hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381778
hg191778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195862
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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