A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616836



Internal ID20989907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43542972..43544905hg38UCSC Ensembl
chr7:43582571..43584504hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381934
hg191934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154565
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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