A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154453



Internal ID20721493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41715054..41715408hg38UCSC Ensembl
chr7:41754652..41755006hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607892
Supporting Variants
Samples
Known GenesINHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00169


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