A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398176



Internal ID21055729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6147324..6182328hg38UCSC Ensembl
chr6:6147557..6182561hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3835005
hg1935005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145561
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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