A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436733



Internal ID21094286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31386881..31394579hg38UCSC Ensembl
chr10:31675810..31683508hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387699
hg197699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979181
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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