A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617502



Internal ID20990573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40048595..40049102hg38UCSC Ensembl
chr7:40088194..40088701hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156816
Samples
Known GenesCDK13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617502
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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