A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614243



Internal ID20987314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19727101..19728200hg38UCSC Ensembl
chr7:19766724..19767823hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156785
Samples
Known GenesTMEM196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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