A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436617



Internal ID21094170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35180921..35372783hg38UCSC Ensembl
chr10:35469849..35661711hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38191863
hg19191863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194243
Samples
Known GenesCCNY, CREM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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