A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156463



Internal ID20723503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37994954..39229437hg38UCSC Ensembl
chr7:38034556..39269036hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381234484
hg191234481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602673
Supporting Variants
Samples
Known GenesAMPH, FAM183B, POU6F2, STARD3NL, TARP, TRG-AS1, VPS41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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