A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541604



Internal ID20914886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35510714..35512288hg38UCSC Ensembl
chr1:35976315..35977889hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv158n223
Supporting Variantsnssv18250408
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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