A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611999



Internal ID20985070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44179560..44180292hg38UCSC Ensembl
chr7:44219159..44219891hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154596
Samples
Known GenesGCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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