A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439717



Internal ID21097270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31752107..31759261hg38UCSC Ensembl
chr10:32041035..32048189hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387155
hg197155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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