A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603937



Internal ID20977008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34979001..34980000hg38UCSC Ensembl
chr7:35018613..35019612hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153093
Samples
Known GenesDPY19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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