A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605804



Internal ID20978875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115174901..115178200hg38UCSC Ensembl
chr7:114814955..114818254hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7093n223
Supporting Variantsnssv18149961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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