A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413050



Internal ID21070603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70859043..70859782hg38UCSC Ensembl
chr6:71568746..71569485hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145082
Samples
Known GenesSMAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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