A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436832



Internal ID21094385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11759026..11783567hg38UCSC Ensembl
chr10:11801025..11825566hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3824542
hg1924542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978321
Samples
Known GenesECHDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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