A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357413



Internal ID21014966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8433756..8522942hg38UCSC Ensembl
chr3:8475442..8564628hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3889187
hg1989187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103229
Samples
Known GenesLMCD1, LMCD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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