A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434338



Internal ID21091891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156887221..156888136hg38UCSC Ensembl
chr7:156679915..156680830hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151480
Samples
Known GenesLMBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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