A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156521



Internal ID20723561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38440301..38441600hg38UCSC Ensembl
chr7:38479901..38481200hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610993
Supporting Variants
Samples
Known GenesAMPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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